DayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe
Cas:90-43-7
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
inquiryProduct Detail Minimum Order Qty. 10 Gram
Cas:90-43-7
Min.Order:10 Gram
Negotiable
Type:Trading Company
inquiryWelcome to Simagchem, your partner in China as a premier supply of bulk specialty chemicals for industry and life science. We introduce experienced quality product and exceptional JIT service with instant market intelligence in China to benefit our
Cas:90-43-7
Min.Order:0 Metric Ton
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Type:Manufacturers
inquiry1. High purity: 99.9% min. 2. Good appearance: white crystalline flakes. 3. No odor, no solvent, no stabilizer. 4. Alkaline solubility: clear and transparent. Specification of CAS:90-43-7 2-Phenylphenol:
Cas:90-43-7
Min.Order:1 Kilogram
FOB Price: $16.0 / 18.0
Type:Other
inquiryUnique advantages for O-Phenylphenol Cas 90-43-7 Guaranteed the purity High quality & competitive price Quality control Fast feedback Prompt shipment Appearance:Flake Storage:0-6°C Package:1kg/foil bag, 25kg/drum or as you require Applica
Cas:90-43-7
Min.Order:1 Kilogram
FOB Price: $20.0 / 220.0
Type:Trading Company
inquiryThe outstanding features and advantages of our 2-phenylphenol: 1. high purity: 99.9% min. 2. good appearance: white crystalline flakes. 3. no odor, no solvent, no stabilizer. 4. alkaline solubility: clear and transparent. 5. Iso9001 ce
Cas:90-43-7
Min.Order:25 Kilogram
Negotiable
Type:Trading Company
inquiryT 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
O-Phenyl phenol Product Name: O-Phenyl phenol Molecular Weight: 170.21 CAS NO: 90-43-7 EC NO: 201-993-5 Molecular Formula: C12H10O
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
Our main production base is located in Xuzhou industry park. We are certified both to the ISO 9001 and ISO 14001 Standards, have a safety management system in place.Our R&D team masters core technology for process-design of target building block
Cas:90-43-7
Min.Order:5 Kiloliter
FOB Price: $1.2 / 5.0
Type:Manufacturers
inquiry2-Phenylphenol Basic information Product Name: 2-Phenylphenol Synonyms: BIPHENYL-2-OL;BIPHENYLOL-2;HYDROXY-(2-PHENYL)BENZENE;FEMA 3959;DOWICIDE 1(R);2-PHENYLPHENOL;2-DIPHENYLOL;2-HYDROXY
Our company has been in existence for 10 years since its establishment. We have our own unique team. The company integrates independent research and development, production and sales. We have established famous brands at home and abroad. At present
Henan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
1.high quality: quality is life. quality is the most important element for all goods. we have a lab doing research in wuhan china. hplc and nmr is available if needed. 2.reasonable price: we provide high quality products wi
Cas:90-43-7
Min.Order:10 Gram
Negotiable
Type:Lab/Research institutions
inquiry2-Phenylphenol CAS: 90-43-7 Specification Molecular Weight 170.2 Physical State Solid (flakes or crystals) Specific Gravity(g/cm3 at 25oC) 1.2 Dissocia
Hangzhou Fanda Chemical Co.,Ltd (FandaChem) , a China-based chemical company, specialize in exporting 2-Phenylphenol;OPP CAS:90-43-7 , Please contact us by email freely. We are leading exporter in China. If you really need this cargo
Cas:90-43-7
Min.Order:0 Metric Ton
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Type:Other
inquiryLorcaserin(856681-05-5)is an orally administered agent and a selective 5-HT2C receptor agonist for the treatment of obesity. It had been approved for marketing in US by FDA on 27 June in 2012. In clinical studies, lorcaserin h
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
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 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:90-43-7
Min.Order:10 Gram
FOB Price: $100.0
Type:Lab/Research institutions
inquirySuperior quality, moderate price & quick delivery. Appearance:white crystals Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:25kg/drum, or as per your request. Application:For medicine , pesticide intermed
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:90-43-7
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
inquiryAppearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
high purity,in stock Package:25kg/drum,or as per customers'demand Application:API,Pharmaceutical intermediates Transportation:air,sea,courier
R & D enterprises have their own stock in stock Package:1kg Application:pharmaceutical intermediates
Q1: Are you a manufacturer Answer: Yes, we are factory founded on 2012.Q2: How to contact with us Click "contact supplier" And then send us message the product you interest in, you will get reply within 12 hours.Q3:Which kind of payment terms do you
Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:90-43-7
Min.Order:1 Kilogram
FOB Price: $112.0
Type:Trading Company
inquiryAnsciep 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
Conditions | Yield |
---|---|
With boron tribromide In dichloromethane at 0 - 25℃; | 100% |
With boron tribromide In dichloromethane at -80℃; |
Conditions | Yield |
---|---|
With palladium chloride*2MeCN; chloranil In 1,4-dioxane at 100℃; for 18h; | 100% |
Multi-step reaction with 2 steps 1: dimethyl sulfoxide; oxygen; palladium(II) trifluoroacetate / acetic acid / 12 h / 80 °C / Reflux; Sealed tube 2: dimethyl sulfoxide; iodine / nitromethane / 24 h / 100 °C / Sealed tube; Green chemistry View Scheme |
Conditions | Yield |
---|---|
With potassium phosphate; SBA-Si-PEG-Pd(PPh3)n In water at 50℃; for 10h; Suzuki coupling; | 99% |
With palladium 10% on activated carbon; potassium carbonate In water at 20 - 80℃; for 18.5h; Suzuki-Miyaura Coupling; Inert atmosphere; | 97% |
With bis(1,1'-ethylene-3,3'-divinylimidazole-2,2'-diylidene)nickel(II) dibromide dihydrate; potassium carbonate In water; N,N-dimethyl-formamide at 100℃; for 8h; Suzuki-Miyaura Coupling; Inert atmosphere; Schlenk technique; | 96% |
6-tert-butyl-6-phenyl-6H-dibenzo[c,e][1,2]oxasiline
2-Phenylphenol
Conditions | Yield |
---|---|
With tetrabutyl ammonium fluoride In tetrahydrofuran at 70℃; for 5h; | 99% |
Conditions | Yield |
---|---|
With methanol; 1,3-disulfonic acid imidazolium hydrogen sulfate at 20℃; for 0.0666667h; Green chemistry; | 99% |
Conditions | Yield |
---|---|
With oxygen; N-ethyl-N,N-diisopropylamine; [5,6]fullerene-C70 In chloroform; toluene at 20℃; for 12h; Irradiation; | 98% |
With N,N-dimethyl-p-toluidine N-oxide In dichloromethane at 20℃; for 0.0166667h; | 95% |
With tert.-butylhydroperoxide; potassium tert-butylate In water at 20 - 50℃; for 5h; | 90% |
Conditions | Yield |
---|---|
With sodium hydride at 190 - 192℃; for 7h; | 92.5% |
With LiCrH4*2LiCl*2THF In tetrahydrofuran at 25℃; for 12h; | 84% |
With lithium aluminium tetrahydride; cobalt acetylacetonate; sodium t-butanolate In toluene at 140℃; for 24h; Inert atmosphere; Sealed tube; | 81% |
Conditions | Yield |
---|---|
With oxygen; triethylamine; sodium iodide In acetonitrile at 32℃; for 24h; Schlenk technique; UV-irradiation; | 91% |
Conditions | Yield |
---|---|
With 5-(di-tert-butylphosphino)-1′, 3′, 5′-triphenyl-1′H-[1,4′]bipyrazole; tris-(dibenzylideneacetone)dipalladium(0); cesiumhydroxide monohydrate In 1,4-dioxane at 110℃; Inert atmosphere; Glovebox; Sealed tube; | 90% |
With water; silica gel; copper(II) oxide at 525 - 600℃; | |
With water; sodium carbonate at 300 - 360℃; |
(Z)-4-phenylocta-1,4,7-trien-3-one
2-Phenylphenol
Conditions | Yield |
---|---|
tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride In dichloromethane at 20℃; for 2h; | 90% |
2-Phenylphenol
Conditions | Yield |
---|---|
With copper; Selectfluor In acetonitrile at 80℃; | 90% |
Conditions | Yield |
---|---|
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In ethanol; water; toluene at 80℃; Suzuki Coupling; Inert atmosphere; Sonication; Reflux; | 89% |
Diethylcarbamic acid, <1,1'-biphenyl>-2-yl ester
2-Phenylphenol
Conditions | Yield |
---|---|
With zirconocene dichloride In tetrahydrofuran at 20℃; Inert atmosphere; | 87% |
With water; sodium hydroxide In ethanol for 8h; Reflux; | 85% |
Conditions | Yield |
---|---|
Stage #1: dibenzothiophene sulfone With sodium hydroxide In water at 300℃; for 1.5h; Autoclave; Stage #2: With hydrogenchloride In water pH=7; Product distribution / selectivity; | 86.5% |
Conditions | Yield |
---|---|
Stage #1: 2-hydroxybromobenzene; phenylmagnesium bromide With tris-(dibenzylideneacetone)dipalladium(0); 4-bromo-phenol; C30H23O2P In tetrahydrofuran at -78 - 25℃; for 2.16667h; Stage #2: With hydrogenchloride In tetrahydrofuran; water | 86% |
With tris-(dibenzylideneacetone)dipalladium(0); 1-bromo-4-methoxy-benzene; C30H23O2P In tetrahydrofuran at -78 - 25℃; Inert atmosphere; | 96 %Spectr. |
([1,1′-biphenyl]-2-yloxy)(tert-butyl)dimethylsilane
2-Phenylphenol
Conditions | Yield |
---|---|
With acetyl chloride In methanol | 86% |
2-iodocyclohex-2-en-1-one
phenylboronic acid
A
2-phenylcyclohex-2-enone
B
2-Phenylphenol
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; sodium carbonate In 1,4-dioxane; water at 20℃; for 24h; Suzuki-Miyaura Coupling; | A 86% B 4% |
N-(phenoxy)-4-methylbenzenesulfonamide
benzene
A
4-Phenylphenol
B
2-hydroxyphenyl p-toluenesulfonimidate
C
toluene-4-sulfonamide
D
2-Phenylphenol
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid; trifluoroacetic acid for 1h; Ambient temperature; Further byproducts given; | A 14% B 13% C 85% D 29% |
N-(phenoxy)-4-methylbenzenesulfonamide
benzene
A
4-Phenylphenol
B
2-hydroxyphenyl p-toluenesulfonimidate
C
toluene-4-sulfonamide
D
4-hydroxyphenyl trifluoromethanesulfonate
E
2-Phenylphenol
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid; trifluoroacetic acid for 1h; Mechanism; Product distribution; Ambient temperature; other N-acyl- and N-sulfonyl-O-arylhydroxylamines under various reaction conditions, different nucleophiles; | A 14% B 13% C 85% D 3% E 29% |
toluene-4-sulfonic acid,2-hydroxyphenyl ester
phenylmagnesium bromide
2-Phenylphenol
Conditions | Yield |
---|---|
Stage #1: phenylmagnesium bromide With C24H52Cl2O12P4Pd2 In tetrahydrofuran; 1,4-dioxane at 20℃; for 0.0833333h; Kumada-Corriu cross-coupling reaction; Inert atmosphere; Stage #2: toluene-4-sulfonic acid,2-hydroxyphenyl ester In tetrahydrofuran; 1,4-dioxane at 110℃; for 24h; Kumada-Corriu cross-coupling reaction; Inert atmosphere; chemoselective reaction; | 84% |
Conditions | Yield |
---|---|
With pyridine In dichloromethane for 3h; | 100% |
With dmap; triethylamine In dichloromethane at 0 - 20℃; for 6h; Schlenk technique; Inert atmosphere; | 98% |
Conditions | Yield |
---|---|
With potassium carbonate In acetone at 60℃; for 20h; | 100% |
With cesium fluoride In acetonitrile at 82℃; | 62% |
With cesium fluoride In acetonitrile at 82℃; | 62% |
Conditions | Yield |
---|---|
With triethylamine; magnesium chloride In tetrahydrofuran for 3h; Heating; | 100% |
Stage #1: formaldehyd; 2-Phenylphenol With triethylamine; magnesium chloride In tetrahydrofuran for 1.7h; Heating / reflux; Stage #2: With hydrogenchloride In water at 0℃; pH=5; | 92% |
With triethylamine; magnesium chloride In tetrahydrofuran at 70℃; for 16h; | 90% |
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 2h; | 100% |
With potassium carbonate In acetone; toluene at 65℃; for 14h; | 95% |
With potassium carbonate In acetone; toluene | 95% |
trifluoromethylsulfonic anhydride
2-Phenylphenol
biphenyl-2-yl trifluoromethanesulfonate
Conditions | Yield |
---|---|
With pyridine In dichloromethane at 0℃; for 2h; | 100% |
With 2,6-dimethylpyridine In dichloromethane at 0 - 20℃; for 2h; Inert atmosphere; | 98% |
With pyridine In dichloromethane at 20℃; for 2h; Inert atmosphere; | 95% |
2-Phenylphenol
p-chlorodibenzo[c.e][1,2]oxaphosphorine
Conditions | Yield |
---|---|
With zinc(II) chloride; phosphorus trichloride at 20 - 180℃; for 7h; | 100% |
With anhydrous phosphorus trichloride; phosphorus trichloride; Zinc chloride In 5,5-dimethyl-1,3-cyclohexadiene | 95% |
Stage #1: 2-Phenylphenol With phosphorus trichloride at 140℃; for 5h; Inert atmosphere; Neat (no solvent); Stage #2: With zinc(II) chloride at 210℃; for 3h; Inert atmosphere; Neat (no solvent); | 90% |
titanium tetrachloride
2-Phenylphenol
trichloro mono(2-phenylphenoxide) titanium(IV)
Conditions | Yield |
---|---|
In dichloromethane byproducts: HCl; under N2; 2-phenylphenol in CH2Cl2 added to TiCl4 (molar ratio 1:1) in CH2Cl2; refluxed for 12.5 h; filtered; solvent removed; dried under vac. for 4 h; elem. anal.; | 100% |
titanium tetrachloride
2-Phenylphenol
[dichlorobis(2-phenylphenolate)titanium(IV)]
Conditions | Yield |
---|---|
In toluene byproducts: HCl; N2, vigorously refluxed for 12 h; cooled, filtered, solvent removed; | 100% |
Conditions | Yield |
---|---|
With potassium hexamethylsilazane In toluene | 100% |
Conditions | Yield |
---|---|
With sulfuric acid In water for 1h; Reflux; | 100% |
Conditions | Yield |
---|---|
With potassium carbonate In dimethyl sulfoxide at 95℃; for 24h; | 100% |
Stage #1: 2-Phenylphenol With sodium hydride In N,N-dimethyl-formamide at 20℃; for 1h; Inert atmosphere; Stage #2: ortho-nitrofluorobenzene In N,N-dimethyl-formamide at 20 - 50℃; for 13h; Inert atmosphere; | 83% |
N,N-diisopropylcarbamoyl chloride
2-Phenylphenol
Conditions | Yield |
---|---|
With sodium hydride In tetrahydrofuran at 20℃; for 12h; Sealed tube; | 100% |
Conditions | Yield |
---|---|
With potassium carbonate at 160℃; for 1h; Temperature; Reagent/catalyst; | 99.2% |
N,N-diethylcarbamyl chloride
2-Phenylphenol
Diethylcarbamic acid, <1,1'-biphenyl>-2-yl ester
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile for 3h; Inert atmosphere; Reflux; | 99% |
With potassium carbonate In acetonitrile for 7h; Heating; | 95% |
With potassium carbonate In acetonitrile for 8h; Reflux; |
Conditions | Yield |
---|---|
With hydrogenchloride; 3-mercaptopropionic acid In water at 80℃; Reagent/catalyst; Inert atmosphere; | 99% |
With hydrogenchloride for 18h; Heating; | 42% |
With methanol; sulfuric acid; 1-dodecylthiol In toluene at 40℃; for 2.5h; Inert atmosphere; | 9 %Chromat. |
2-Phenylphenol
Isopropyl isocyanate
O-2-biphenylyl N-isopropylcarbamate
Conditions | Yield |
---|---|
With dmap In tetrahydrofuran at 60℃; for 24h; | 99% |
2-Phenylphenol
dibenzo[c,e][1,2]oxaborinin-6-ol
Conditions | Yield |
---|---|
With boron trichloride; aluminium trichloride In hexane at 70 - 75℃; for 6h; | 99% |
Multi-step reaction with 2 steps 1: (i) BCl3, CH2Cl2, (ii) AlCl3, PE 2: Et2O / light petroleum View Scheme | |
With boron trichloride |
2-Phenylphenol
3-bromo[1,1’-biphenyl]-2-ol
Conditions | Yield |
---|---|
With N-bromo-tert-butylamine In chloroform at 0℃; Inert atmosphere; | 99% |
With N-Bromosuccinimide; diisopropylamine In dichloromethane for 16h; Reflux; Inert atmosphere; | 96% |
With N-Bromosuccinimide; diisopropylamine In dichloromethane for 16h; Inert atmosphere; Reflux; | 95% |
Conditions | Yield |
---|---|
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 20℃; for 96h; Mitsunobu reaction; | 99% |
Conditions | Yield |
---|---|
Stage #1: 2-Phenylphenol With potassium tert-butylate In tetrahydrofuran at 0℃; for 0.25h; Stage #2: diphenyliodonium tetrafluoroborate In tetrahydrofuran at 20℃; for 3h; | 99% |
2-Phenylphenol
1-(3-methoxyphenoxy)-2-methylbenzene
Conditions | Yield |
---|---|
Stage #1: 2-Phenylphenol With potassium tert-butylate In tetrahydrofuran at 0℃; for 0.25h; Stage #2: bis(2-methylphenyl)iodonium tetrafluoroborate In tetrahydrofuran at 40℃; for 0.5h; | 99% |
Conditions | Yield |
---|---|
With caesium carbonate In tetrahydrofuran | 99% |
With caesium carbonate In tetrahydrofuran at 20℃; for 12h; | 98% |
Conditions | Yield |
---|---|
Stage #1: 4-tert-Butylcatechol; 4-(4-chlorophenoxy)-3,5,6-trifluorophthalonitrile With potassium carbonate In acetonitrile at 80℃; for 2h; Stage #2: 2-Phenylphenol With potassium carbonate In acetonitrile at 80℃; for 10h; | 99% |
1-iodo-butane
carbon monoxide
2-Phenylphenol
valeric acid biphenyl-2-yl ester
Conditions | Yield |
---|---|
With rhodium(III) chloride; 1,3-bis-(diphenylphosphino)propane; sodium carbonate; sodium bromide In 1,4-dioxane at 120℃; under 750.075 Torr; for 24h; Inert atmosphere; chemoselective reaction; | 99% |
sodium benzenesulfonate
2-Phenylphenol
[1,1’-biphenyl]-2-yl benzenesulfonate
Conditions | Yield |
---|---|
In water; acetonitrile at 20℃; for 2h; Electrochemical reaction; | 99% |
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