Lonwin Chemical Group Limited
Lonwin Industry group limited as a professional manufactor & exporter of chemical materials ,we totally haver more than 270 stuffs, we have been on this line for more than 9 years. Our chemical materials are exported to lot of countries and reg
Cas:108-95-2
Min.Order:100 Kilogram
Negotiable
Type:Other
inquiryDayang Chem (Hangzhou) Co.,Ltd.
Dayangchem's R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. DayangChem can provide different quantities
Wuhan Fortuna Chemical Co.,Ltd
Unique advantages for D-Cycloserine Cas 68-41-7 High quality & competitive price Quality control Fast feedback Prompt shipment Appearance:Colorless to reddish needle crystallization Storage:Store in 2-8℃ Package:25kg/drum Application:m
Cas:108-95-2
Min.Order:1 Kilogram
FOB Price: $105.0 / 120.0
Type:Trading Company
inquiryHebei yanxi chemical co.,LTD.
Hebei yanxi chemical co., LTD is a professional research, development and production Cyromazine、lead diacetate trihydrate /Lead acetate trihydrateC、 2-phenylacetamide 、 4-Aminophenyl-1-phenethylpiperidine 、Citric acid monohydrate 、 Citric acid/c
Henan Allgreen Chemical Co.,Ltd
T he company has advanced technology, as well as a large number of excellent R & D team, to provide customers from the grams to one hundred kilograms and tons of high-quality products, competitive prices and quality service Appearance:White or
Ality Chemical Corporation
The above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
Chemwill Asia Co., Ltd.
Highly quality and large production Factory Chemwill Asia co.,Ltd is one of the leading manufacturer in CHINA. Our main production base is located in Xuzhou industry park. We produce a wide range of organics includin
Henan Tianfu Chemical Co., Ltd.
Our company was built in 2009 with an ISO certificate.In the past 6 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so
Cas:108-95-2
Min.Order:1 Metric Ton
FOB Price: $500.0
Type:Lab/Research institutions
inquiryHenan Sinotech Import&Export Corporation
Product information Product Name Phenol CAS No. 108-95-2 Chemical formula
Hubei Langyou International Trading Co., Ltd
1. Guaranteed purity; 2. Large quantity in stock; 3. Largest manufacturer; 4. Best service after shipment with email; 5. High quality & competitive price; Appearance:White Crystalline Powder Storage:Store in sealed conta
Cas:108-95-2
Min.Order:10 Gram
Negotiable
Type:Other
inquiryChangchun Artel lmport and Export trade company
Product Detail Minimum Order Qty. 10 Gram
Cas:108-95-2
Min.Order:10 Gram
Negotiable
Type:Trading Company
inquiryHebei Mojin Biotechnology Co.,Ltd
Company information: Hebei Mojin Biotechnology Co., Ltd, Our company is a professional in carbomer,carbopol,lead acetate,meglumine diphenyl ethylamine and other chemical raw materials and chemical reagents research and development production ente
Cas:108-95-2
Min.Order:1 Kilogram
FOB Price: $20.0 / 30.0
Type:Trading Company
inquiryWuhan Zenuo Biological Medicine Technology Co Ltd
Product Name: Phenol Synonyms: PHENOL, LIQUIDPHENOL, LIQUIDPHENOL, LIQUID;PHENOL, REAGENT (ACS), LOOSE CRYSTALSPHENOL, REAGENT (ACS), LOOSE CRYSTALSPHENOL, REAGENT (ACS), LOOSE CRYSTALS;PHENOL LOOSE XTL;Phenol equilibrated, stablilized;Phenol wat
Cas:108-95-2
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
inquiryTriumph International Development Limilted
Appearance:White granular powder Storage:Store in a cool,dry place and keep away from direct strong light Package:As customer request Application:Phenol is an antiseptic and disinfecta... Transportation:Common products:Sea/Air/
Hangzhou Keyingchem Co.,Ltd
Hangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
Hangzhou J&H Chemical Co., Ltd.
J&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
Zibo Hangyu Biotechnology Development Co., Ltd
Zibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi
Cas:108-95-2
Min.Order:10 Gram
FOB Price: $100.0
Type:Lab/Research institutions
inquiryZibo Dorne chemical technology co. LTD
Product Details Grade: pharmaceutical grade Purity:99%+ ProductionCapacity: 1000 Kilogram/Month Scope of use: For scientific research only(The product must be used legally) Our Advantage 1. Best quality with competitive price. 2. Quick shipping,
Cas:108-95-2
Min.Order:1 Metric Ton
Negotiable
Type:Lab/Research institutions
inquirySiwei Development Group Ltd.
Product name: Phenol CAS No.：108-95-2 Molecule Formula：C6H6O Molecule Weight：94.11 Purity: 99.0% Package: 25kg/drum Description：White crystalline powder Manufacture Standards：Enterprise Standard TESTING ITEMS
Henan Wentao Chemical Product Co., Ltd.
1)quick response within 12 hours; 2)quality guarantee: all products are strictly tested by our qc, confirmed by qa and approved by third party lab in china, usa, canada, germany, uk, italy, france etc. 3) oem/odm available; 4) rea
Cas:108-95-2
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
inquiryHangzhou Huarong Pharm Co., Ltd.
Hangzhou Huarong Pharm Co., Ltd.established since 2006 , has been actively developing specialty products for Finished Dosages, APIs, Intermediates, and Fine chemicals markets in North America, Europe, Korea, Japan, Mid-East and all over the World. Hu
Hunan chemfish Pharmaceutical co.,Ltd
Appearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
SAGECHEM LIMITED
SAGECHEM is a chemical R&D, manufacturing and distribution company in China since 2009, including pharmaceutical intermediates, agrochemical, dyestuff intermediates, organosilicone, API and etc. We also offer a full range of services in custom synthe
HANGZHOU YUNUO CHEMICAL CO.,LTD
Superior quality, moderate price & quick delivery. Appearance:white crystalline powder Storage:stored in a cool, dry and ventilated place to provent sun and rain Package:25kg/drum, or as per your request. Application: Used in organic synthe
Kono Chem Co.,Ltd
high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
GIHI CHEMICALS CO.,LIMITED
high purity,in stock Package:25kg/drum,or as per customers'demand Application:API,or Intermediates,fine chemicals Transportation:air,sea,courier
JINHUA HUAYI CHEMICAL CO., LTD.
Jinhua huayi chemical co., ltd. is dedicated to the development, production and marketing of chemicals. On the basis of equality and mutual benefit, and under the principle of customer first, credit first, quality first, we are ready to join hands
Aecochem Corp.
Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
Zhuozhou Wenxi import and Export Co., Ltd
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:108-95-2
Min.Order:1 Kilogram
FOB Price: $112.0
Type:Trading Company
inquiryAntimex Chemical Limied
Ansciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
Synthetic route
| Conditions | Yield |
|---|---|
| With potassium tert-butylate; N,N-dimethyl-formamide at 35℃; for 24h; Schlenk technique; Inert atmosphere; Irradiation; | 100% |
| With tris-(trimethylsilyl)silane In acetonitrile for 24h; Schlenk technique; Inert atmosphere; Irradiation; | 98% |
| With aluminium trichloride In dichloromethane; ethanethiol for 0.15h; Mechanism; Ambient temperature; var. other halogenated phenols; | 86.7% |
| With potassium phosphate; palladium diacetate; hydrazine hydrate In dimethyl sulfoxide; N,N-dimethyl-formamide at 20℃; for 8h; Green chemistry; | 68% |
| Conditions | Yield |
|---|---|
| montmorillonite K-10 for 0.0166667h; Product distribution; Further Variations:; Catalysts; Solid phase reaction; desilylation; microwave irradiation; | 100% |
| With bismuth(lll) trifluoromethanesulfonate In methanol at 20℃; for 0.0333333h; | 98% |
| With methanol; 1,3-disulfonic acid imidazolium hydrogen sulfate at 20℃; for 0.0666667h; Green chemistry; | 98% |
| Conditions | Yield |
|---|---|
| With bis(1,5-cyclooctadiene)nickel (0); triphenylphosphine at 54℃; for 20h; Product distribution; Rate constant; Thermodynamic data; other solvents, reagents, reagents ratio, time, temperature; activation energy, ΔH<*>, ΔS<*>; | A 100% B n/a C 100% |
| Conditions | Yield |
|---|---|
| With phosphate buffer; Phenyl acetate In diethyl ether for 2.75h; Ambient temperature; pig liver acetone powder; | A 5% B 100% |
-
-
50972-20-8
phenyl-α-chloroethyl-carbonate
-
A
-
109548-52-9
phenyl 1-thiocyanoethylcarbonate
-
B
-
108-95-2
phenol
| Conditions | Yield |
|---|---|
| In formamide for 72h; Ambient temperature; | A 100% B 35% |
| Conditions | Yield |
|---|---|
| With thallous phenoxide In diethyl ether for 24h; | A 100% B 94% |
| Conditions | Yield |
|---|---|
| With aluminium(III) iodide; tetra-(n-butyl)ammonium iodide In cyclohexane for 0.3h; Heating; | 100% |
| With water; hydrogen bromide; Aliquat 336 at 105℃; for 5h; Catalytic behavior; | 96% |
| With monochloroborane dimethyl sulfide complex In benzene Heating; | 95% |
| Conditions | Yield |
|---|---|
| With hydrogen; sodium hydroxide In water under 760.051 Torr; for 0.833333h; Kinetics; Reagent/catalyst; Solvent; Green chemistry; | 100% |
| With hydrogen; sodium hydroxide In water at 20℃; for 2h; Kinetics; Catalytic behavior; Solvent; Reagent/catalyst; | 99.1% |
| With hydrogen; sodium hydroxide In water at 25℃; under 760.051 Torr; for 2h; Reagent/catalyst; Solvent; | 99.9% |
-
-
105930-58-3
7,7,8,8-Tetramethyl-3-methylene-5-phenoxy-1,4,6,9-tetraoxa-5λ5-phospha-spiro[4.4]nonan-2-one
-
A
-
13882-05-8
2-hydroxy-4,4,5,5-tetramethyl<1,3,2>dioxaphospholane-2-oxide
-
B
-
127-17-3
2-oxo-propionic acid
-
C
-
108-95-2
phenol
| Conditions | Yield |
|---|---|
| With water In acetone at 20℃; for 24h; | A 100% B n/a C n/a |
| Conditions | Yield |
|---|---|
| With HZSM-5(30) In water for 7h; Product distribution; Heating; var. catalysts; other acetylated alcohols; | 100% |
| silica gel; toluene-4-sulfonic acid In water; toluene at 80℃; for 6h; | 100% |
| With sodium hydrogen telluride; acetic acid In ethanol for 0.5h; Heating; | 100% |
| Conditions | Yield |
|---|---|
| With phosphate buffer; Phenyl acetate In diethyl ether for 2.75h; Ambient temperature; pig liver acetone powder; | A 18% B 100% |
| Conditions | Yield |
|---|---|
| With phosphate buffer; Phenyl acetate In diethyl ether for 2.75h; Ambient temperature; pig liver acetone powder; | A 9% B 100% |
| Conditions | Yield |
|---|---|
| With perchloric acid In diethyl ether; water at 20℃; for 0.166667h; | 100% |
| With samarium diiodide In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide at 20℃; for 0.0833333h; Etherification; | 99.3% |
| With sodium hydroxide In water at 20℃; | 91% |
| Conditions | Yield |
|---|---|
| H6P2W18O62; silica gel In tetrahydrofuran; methanol at 65℃; for 0.916667h; Product distribution; Further Variations:; Catalysts; | 100% |
| With bismuth(III) chloride In water; acetonitrile at 50℃; for 1h; Reagent/catalyst; Solvent; Temperature; | 95% |
| sodium hydrogen sulfate; silica gel In dichloromethane at 20℃; for 1.5h; | 94% |
-
-
1295-35-8
bis(1,5-cyclooctadiene)nickel (0)
-
-
15133-82-1
tetrakis(triphenylphosphine)nickel(0)
-
B
-
15376-83-7
(triphenylphosphine)3(CO)nickelk
-
C
-
74-85-1
ethene
-
D
-
108-95-2
phenol
| Conditions | Yield |
|---|---|
| With triphenylphosphine In neat (no solvent) (N2 or Ar or vac.), EtCOOPh added to Ni(cod)2 and Ni(PPh3)4, mixture stirred at 54°C for 20 h; GLC; | A 73% B n/a C 100% D 91% |
-
-
1295-35-8
bis(1,5-cyclooctadiene)nickel (0)
-
-
637-27-4
phenyl propionate
-
A
-
15376-83-7
(triphenylphosphine)3(CO)nickelk
-
B
-
74-85-1
ethene
-
C
-
108-95-2
phenol
| Conditions | Yield |
|---|---|
| With triphenylphosphine In neat (no solvent) Kinetics; byproducts: diethyl ketone, 1,3-cyclooctadiene, 1,4-cyclooctadiene; further byproducts: 1,5-cyclooctadiene, bicyclooctene-1, bicyclooctene-2, (N2 or Ar or vac.), EtCOOPh added to Ni(cod)2 and PPh3 (PPh3/Ni = 10), mixture stirred at 54°C for 21 h; gas chromy., volatile removed in vac., recrystd. from THF-hexane; | A 80% B 100% C 100% |
| With triphenylphosphine In neat (no solvent) Kinetics; byproducts: diethyl ketone, 1,3-cyclooctadiene, 1,4-cyclooctadiene; further byproducts: 1,5-cyclooctadiene, bicyclooctene-1, bicyclooctene-2, (N2 or Ar or vac.), EtCOOPh added to Ni(cod)2 and PPh3 (PPh3/Ni = 4),mixture stirred at 54°C for 20 h; gas chromy., volatile removed in vac., recrystd. from THF-hexane; | A 60% B 100% C 100% |
| With triphenylphosphine In neat (no solvent) Kinetics; byproducts: diethyl ketone, 1,3-cyclooctadiene, 1,4-cyclooctadiene; further byproducts: 1,5-cyclooctadiene, bicyclooctene-1, bicyclooctene-2, (N2 or Ar or vac.), EtCOOPh added to Ni(cod)2 and PPh3 (PPh3/Ni = 3),mixture stirred at 54°C for 20 h; gas chromy., volatile removed in vac., recrystd. from THF-hexane; | A 60% B 90% C 90% |
| With triphenylphosphine In neat (no solvent) Kinetics; byproducts: diethyl ketone, 1,3-cyclooctadiene, 1,4-cyclooctadiene; further byproducts: 1,5-cyclooctadiene, bicyclooctene-1, bicyclooctene-2, (N2 or Ar or vac.), EtCOOPh added to Ni(cod)2 and PPh3 (PPh3/Ni = 2),mixture stirred at 54°C for 12 h; gas chromy., volatile removed in vac., recrystd. from THF-hexane; | A 30% B 60% C 60% |
| With triphenylphosphine In neat (no solvent) Kinetics; byproducts: diethyl ketone, 1,3-cyclooctadiene, 1,4-cyclooctadiene; further byproducts: 1,5-cyclooctadiene, bicyclooctene-1, bicyclooctene-2, (N2 or Ar or vac.), EtCOOPh added to Ni(cod)2 and PPh3 (PPh3/Ni = 1),mixture stirred at 54°C for 12 h; gas chromy., volatile removed in vac., recrystd. from THF-hexane; | A n/a B 40% C 50% |
-
-
1295-35-8
bis(1,5-cyclooctadiene)nickel (0)
-
-
637-27-4
phenyl propionate
-
-
1038-95-5
Tri(p-tolyl)phosphine
-
A
-
74-85-1
ethene
-
B
-
74887-07-3
Ni(CO)(P(C6H4CH3)3)3
-
C
-
108-95-2
phenol
| Conditions | Yield |
|---|---|
| In further solvent(s) Kinetics; (N2 or Ar or vac.), EtCOOPh added to Ni(cod)2 and P(C6H4CH3)3 (P(Ph-CH3)3/Ni = 3) in acetophenone, mixture stirred at 65°C for 50 h; | A 80% B 85% C 100% |
| Conditions | Yield |
|---|---|
| With aluminum (III) chloride; diphenyl diselenide; zinc In acetonitrile at 70℃; for 19.25h; | 100% |
-
-
24388-23-6
2-phenyl-4,4,5,5-tetramethyl-1,3,2-dioxoborole
-
-
108-95-2
phenol
| Conditions | Yield |
|---|---|
| With urea hydrogen peroxide adduct In methanol at 27 - 29℃; for 0.25h; Green chemistry; chemoselective reaction; | 100% |
| With dihydrogen peroxide; 1-butyl-3-methylimidazolium chloride In water at 20℃; for 0.5h; Green chemistry; | 97% |
| With water; 3-chloro-benzenecarboperoxoic acid In ethanol at 20℃; for 6h; | 96% |
-
-
108-95-2
phenol
| Conditions | Yield |
|---|---|
| With urea hydrogen peroxide adduct In methanol at 27 - 29℃; for 0.25h; Green chemistry; chemoselective reaction; | 100% |
| With Oxone; water In acetone at 20℃; for 0.0333333h; | 96% |
| With LACTIC ACID; dihydrogen peroxide In water at 20℃; for 0.166667h; Green chemistry; | 89% |
| Conditions | Yield |
|---|---|
| With C5H11N*Cu(2+)*2NO3(1-); water at 30℃; for 2h; | 100% |
| With water at 60℃; for 5h; Green chemistry; | 100% |
| With water; oxygen; sodium sulfite at 50℃; for 1h; Temperature; Green chemistry; | 100% |
-
-
54897-52-8
phenyl 3,3-dimethylacrylate
-
-
108-95-2
phenol
| Conditions | Yield |
|---|---|
| With perchloric acid In acetonitrile at 20℃; for 1.25h; photo-Fries rearrangement; Inert atmosphere; Irradiation; | 100% |
-
-
16156-59-5
phenyl methanesulfonate
-
-
108-95-2
phenol
| Conditions | Yield |
|---|---|
| With sodium phosphate In aq. phosphate buffer; water; dimethyl sulfoxide at 25℃; for 0.333333h; pH=7.5; Enzymatic reaction; | 100% |
-
-
89466-08-0
2-hydroxyphenyl boronic acid
-
-
108-95-2
phenol
| Conditions | Yield |
|---|---|
| In dimethylsulfoxide-d6 at 120℃; for 2h; Suzuki Coupling; Inert atmosphere; | 100% |
| In dimethyl sulfoxide at 120℃; for 4h; Solvent; Temperature; | 100% |
| In dimethyl sulfoxide at 120℃; for 4h; Solvent; Temperature; Time; Reagent/catalyst; | 95% |
| With N-methyliminodiacetic acid In dimethyl sulfoxide; toluene at 120℃; for 12h; Inert atmosphere; Molecular sieve; | |
| With 3-methyl-5H-1,4,2-dioxazol-5-one; Cp*Rh(OAc)2*H2O In tetrahydrofuran at 20℃; for 12h; Schlenk technique; Inert atmosphere; Sealed tube; |
-
-
108-95-2
phenol
| Conditions | Yield |
|---|---|
| With water In dimethyl sulfoxide at 120℃; for 24h; Time; Reagent/catalyst; | 100% |
| In dimethyl sulfoxide at 120℃; for 12h; | 96% |
| Multi-step reaction with 2 steps 1: dimethyl sulfoxide; toluene / 12 h / Molecular sieve; Reflux; Dean-Stark 2: dimethyl sulfoxide / 240 h / 120 °C View Scheme |
-
-
269409-97-4
2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
-
-
108-95-2
phenol
| Conditions | Yield |
|---|---|
| In dimethyl sulfoxide at 120℃; for 24h; | 100% |
| In dimethyl sulfoxide at 120℃; for 24h; | 96% |
-
-
71597-85-8
(p-hydroxyphenyl)boronic acid
-
-
108-95-2
phenol
| Conditions | Yield |
|---|---|
| With acetic acid In 1,4-dioxane at 100℃; Reagent/catalyst; Solvent; Enzymatic reaction; | 100% |
| In formic acid at 60℃; for 2h; | 82% |
| With acetic acid at 130℃; for 1h; Reagent/catalyst; Temperature; Green chemistry; | 81% |
| With [bis(trifluoromethanesulfonyl)imidate](triphenylphosphine)gold(I) In toluene at 70℃; for 1.5h; Temperature; Microwave irradiation; Green chemistry; | 65% |
| Conditions | Yield |
|---|---|
| With boron tribromide In dichloromethane | 100% |
| Conditions | Yield |
|---|---|
| With Ni0.85Rh0.15; hydrogen In water at 95℃; under 760.051 Torr; for 16h; Reagent/catalyst; | A 100% B 5% C 79% |
| With isopropyl alcohol at 150℃; under 7500.75 Torr; for 48h; Inert atmosphere; Autoclave; | A 100% B 12.2% C 87.5% |
| With isopropyl alcohol at 150℃; under 7500.75 Torr; for 3h; Catalytic behavior; Temperature; Inert atmosphere; Autoclave; | A 100% B 73.1% C 22.4% |
| With Ru0.6Ni0.4; hydrogen In water at 95℃; under 760.051 Torr; for 16h; Reagent/catalyst; | A 98% B 61% C 6% |
| With hydrogen In n-heptane at 140℃; under 750.075 Torr; for 6h; Catalytic behavior; | A 34 %Chromat. B 12 %Chromat. C 22 %Chromat. |
| Conditions | Yield |
|---|---|
| With cerium(III) chloride; sodium iodide at 25℃; for 26h; | 100% |
| With poly-p-styryl-acetonyltriphenylphosphonium bromide In dichloromethane at 20℃; for 3h; | 99% |
| With zirconium(IV) chloride In dichloromethane for 1h; | 99% |
| Conditions | Yield |
|---|---|
| With copper; caesium carbonate In N,N-dimethyl-formamide at 100℃; for 0.166667h; Ullmann Condensation; Microwave irradiation; Inert atmosphere; | 100% |
| With 1,1,1,5,5,5-hexafluoroacetylacetone; copper(II) ferrite; caesium carbonate In 1-methyl-pyrrolidin-2-one at 135℃; for 24h; Ullmann Condensation; Inert atmosphere; Schlenk technique; | 99% |
| With 2-acetonylpyridine; caesium carbonate; copper(I) bromide In dimethyl sulfoxide at 90℃; for 15h; Inert atmosphere; chemoselective reaction; | 98% |
| Conditions | Yield |
|---|---|
| With erbium(III) triflate In diethyl ether at 25℃; for 24h; | 100% |
| With BiCl6(3-)*2C4H10N2*ClH*3H(1+)*H2O In neat (no solvent) at 20℃; for 0.166667h; | 90% |
| With toluene-4-sulfonic acid; toluene Trennung von (+-)-1-Phenoxy-1-phenyl-aethanol-(2) und (+-)-2-Phenoxy-1-phenyl-aethanol-(1) ueber die 2-Carboxy-benzoyl-Derivate; | |
| In benzene | |
| Stage #1: phenol With sodium hydroxide In water at 80℃; for 0.166667h; Stage #2: styrene oxide In water at 100℃; for 3h; Reagent/catalyst; | 15.0 g |
| Conditions | Yield |
|---|---|
| With sodium hydride In tetrahydrofuran at 20℃; | 100% |
| With sodium hydride In tetrahydrofuran at 20℃; | 99% |
| With potassium carbonate In N,N-dimethyl-formamide at 80℃; | 97% |
| Conditions | Yield |
|---|---|
| With pyridine In toluene at 220℃; for 24h; | 100% |
| With pyridine | 97% |
| With pyridine In toluene at 20 - 100℃; for 1h; | 65.2% |
| Conditions | Yield |
|---|---|
| With pyridine; aluminum oxide at 103 - 105℃; for 2h; microwave irradiation; | 100% |
| With 2,6-di-tert-butyl-pyridine; sodium tetracarbonyl cobaltate In acetonitrile for 12h; | 100% |
| With SBA-15-Ph-Pr-SO3H at 20℃; for 0.25h; | 100% |
| Conditions | Yield |
|---|---|
| With tetrabutyl-ammonium chloride; sodium hydroxide In dichloromethane; water at 0℃; for 0.0833333h; | 100% |
| zinc(II) chloride In toluene | 99% |
| With sodium hydride In tetrahydrofuran at 20℃; for 1h; | 98% |
| Conditions | Yield |
|---|---|
| at 20℃; for 2h; | 100% |
| With cesium fluoride | 93.1% |
| With triethylamine In acetonitrile for 24.5h; Esterification; | 89% |
| Conditions | Yield |
|---|---|
| With triethylamine In benzene at 10℃; Kinetics; Mechanism; Thermodynamic data; Various temperatures, various concentrations. E(act.), ΔS(act.); | 100% |
| With triethylamine In dichloromethane at -15℃; for 1h; Green chemistry; | 100% |
| With triethylamine In ethyl acetate at 0 - 20℃; for 0.166667h; Green chemistry; | 97% |
| Conditions | Yield |
|---|---|
| With 1,4-diaza-bicyclo[2.2.2]octane In dichloromethane at 20℃; for 12h; Inert atmosphere; | 100% |
| With dmap In dichloromethane at 20℃; for 3h; Inert atmosphere; | 99% |
| dmap In dichloromethane at 20℃; for 2h; | 81% |
| With diethyl ether; triethylamine |
| Conditions | Yield |
|---|---|
| With cesium fluoride/clinoptilolite In dimethyl sulfoxide at 110℃; for 0.15h; Reagent/catalyst; Solvent; Temperature; Ullmann Condensation; | 100% |
| With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 17h; | 100% |
| With potassium fluoride on basic alumina; 18-crown-6 ether In acetonitrile for 1h; Heating; | 98% |
| Conditions | Yield |
|---|---|
| With sodium hydroxide In tetrahydrofuran; water at 0 - 20℃; for 2h; Green chemistry; | 100% |
| With potassium carbonate for 0.05h; microwave irradiation; | 99% |
| With sodium carbonate In water at 20℃; for 3h; Catalytic behavior; Reagent/catalyst; | 99% |
| Conditions | Yield |
|---|---|
| With hydrogenchloride at 15 - 20℃; for 3h; | 100% |
| With hydrogenchloride |
| Conditions | Yield |
|---|---|
| With tetrabutyl-ammonium chloride; sodium hydroxide In dichloromethane; water at 0℃; for 0.0833333h; | 100% |
| Conditions | Yield |
|---|---|
| Stage #1: phenol With sodium hydroxide In water at 25℃; for 0.666667h; Stage #2: epichlorohydrin In water at 30 - 35℃; for 16h; | 100% |
| With n-Bu4NOSO2OCH2CHOHCH3; potassium carbonate at 75 - 80℃; for 1.5h; | 91% |
| With n-BuNOSO2OCH2CHOHCH3; potassium carbonate at 75 - 80℃; for 1.5h; other aryl alcohols, var. phase transfer catalysts, var. reaction time; | 91% |
| Conditions | Yield |
|---|---|
| With potassium hydroxide; acyclic polyethylene oxides In dichloromethane; water for 0.5h; | 100% |
| With aluminum oxide; potassium fluoride In N,N-dimethyl-formamide for 1h; Product distribution; Ambient temperature; other phenols and alcohols, other alkylating agents, other reagents and solvents, var. time; | 100% |
| With potassium hydroxide; Aliquat 336 at 20℃; for 5h; | 99% |
| Conditions | Yield |
|---|---|
| With triethylamine In dichloromethane at 23℃; for 2h; Inert atmosphere; | 100% |
| With dmap In tetrahydrofuran at 60℃; for 24h; | 94% |
| With dmap In tetrahydrofuran Heating; | 94% |
| With aluminium trichloride |
| Conditions | Yield |
|---|---|
| With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃; | 100% |
| Stage #1: phenylacetic acid With phosphoric acid; trifluoroacetic anhydride In acetonitrile at 25℃; for 0.5h; Stage #2: phenol In acetonitrile at 25℃; for 20h; | 93% |
| Stage #1: phenylacetic acid With (E)-ethyl 2-cyano-2-(2-nitrophenylsulfonyloxyimino)acetate; N-ethyl-N,N-diisopropylamine In dichloromethane at 25℃; Stage #2: phenol In dichloromethane at 25℃; | 87% |
| Conditions | Yield |
|---|---|
| at 170℃; | 100% |
| With potassium carbonate In N,N-dimethyl-formamide at 60℃; for 1h; Williamson Ether Synthesis; Darkness; Inert atmosphere; | 97% |
| With sodium hydroxide In N-methyl-acetamide; water | 75% |
| Conditions | Yield |
|---|---|
| With ethylaluminum dichloride bis(2-chloroethyl) ether complex In hexane; Cyclohexane-d12 at 25℃; for 2.5h; Catalytic behavior; Friedel-Crafts Alkylation; Glovebox; Inert atmosphere; regioselective reaction; | 100% |
| bei Siedetemperatur; | |
| at 75℃; unter Druck; |
| Conditions | Yield |
|---|---|
| With Hexamethylphosphorous triamide In toluene at 130℃; for 8h; Schlenk technique; Sealed tube; Inert atmosphere; regioselective reaction; | 100% |
| With phosphorus trichloride at 35 - 160℃; under 7.50075 Torr; for 6h; Temperature; Flow reactor; Inert atmosphere; | 94% |
| With 1H-imidazole; carbon disulfide; Hexamethylphosphorous triamide In benzene at 20 - 25℃; for 24h; | 86% |
| Conditions | Yield |
|---|---|
| With benzyltriphenylphosphonium peroxodisulfate; potassium bromide In acetonitrile for 4.5h; Heating; | 100% |
| With sulfuric acid; C20H22Br2N2O5V; dihydrogen peroxide In methanol; water at 20℃; for 1.33333h; Catalytic behavior; | 100% |
| With oxygen; sodium bromide In dibutyl ether at 45℃; under 760.051 Torr; for 5h; Schlenk technique; | 99% |
-
-
108-95-2
phenol
-
-
42368-15-0
(4-hydroxyphenyl)tellurium trichloride
| Conditions | Yield |
|---|---|
| With tellurium tetrachloride In tetrachloromethane for 3h; Substitution; Heating; | 100% |
| With tetrachloromethane; tellurium tetrachloride | |
| With tellurium tetrachloride |
| Conditions | Yield |
|---|---|
| With potassium hydride In tetrahydrofuran at 70℃; Inert atmosphere; | 100% |
| With potassium hydroxide In water at 24℃; for 0.5h; | 98% |
| With potassium hydroxide In water for 0.25h; | 98% |
| Conditions | Yield |
|---|---|
| With dihydrogen peroxide; MgAlZr0.1-HT In Petroleum ether at 79.9℃; for 8h; | 100% |
| With 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione In methanol; chloroform at -25℃; for 0.333333h; | 97% |
| With tert.-butylhydroperoxide In water; acetonitrile at 70℃; for 6h; Catalytic behavior; Temperature; Solvent; | 89% |
| Conditions | Yield |
|---|---|
| With CuCl2 In acetonitrile | 100% |
| With [CuII2(μ-OH)(1,2-bis(2-(bis(2-pyridylmethyl)aminomethyl)-6-pyridyl)ethane)](ClO4)3 ; dihydrogen peroxide; triethylamine In water; acetonitrile at 50℃; for 10h; Catalytic behavior; Inert atmosphere; | 99% |
| With manganese(IV) oxide; sulfuric acid; aniline at 10℃; for 1.5h; | 95% |
| Conditions | Yield |
|---|---|
| With hydrogen; tetra(n-butyl)ammonium hydrogensulfate; rhodium colloidal catalyst In water at 36℃; under 180018 Torr; for 62h; pH=7.5; Catalytic hydrogenation; | 100% |
| In methanol; water | 100% |
| With hydrogen In water at 70℃; under 7500.75 Torr; for 0.25h; | 100% |
| Conditions | Yield |
|---|---|
| Stage #1: 4-nitro-aniline With hydrogenchloride; sodium nitrite In water at 2℃; for 1.5h; Stage #2: phenol With sodium hydroxide In water at 2 - 20℃; for 4h; | 100% |
| Stage #1: 4-nitro-aniline With carboxyl- and nitrite- functionalized graphene quantum dots at 20℃; for 0.0833333h; Stage #2: phenol In water at 20℃; for 0.166667h; | 96% |
| Stage #1: 4-nitro-aniline With hydrogenchloride In water; acetone at 0℃; Inert atmosphere; Stage #2: With sodium nitrite In water; acetone at 0℃; for 1h; Inert atmosphere; Stage #3: phenol With sodium carbonate; sodium hydroxide In water; acetone at 0 - 20℃; for 3h; Inert atmosphere; | 92% |
| Conditions | Yield |
|---|---|
| 100% | |
| With dimethylmonochlorosilane; triethylamine for 1h; temp.: below 40 deg C; | 57% |
| With dimethylmonochlorosilane Heating; | |
| at 20 - 160℃; for 2h; Inert atmosphere; |
| Conditions | Yield |
|---|---|
| With dmap; trimethylsilylethoxyacetylene; mercury(II) oxide In 1,2-dichloro-ethane at 40℃; for 0.5h; | 100% |
| With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃; | 100% |
| With dmap; di-2-thienyl carbonate In dichloromethane at 20℃; for 2h; | 95% |
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