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:106-44-5
Min.Order:1 Kilogram
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inquiryProduct description: Product name p-Cresol CAS number 106-44-5 Assay ≥99% Appearance White crystal or colorless liquid Capacity 500mt/year Application Antioxidant, rubber ant
hebei yanxi chemical co., LTD who registered capital of 10 million yuan, nearly to $2 million, we have a pharmaceutical raw materials factory production of pharmaceutical raw materials, and a reagent r&d center, and we do research and developm
Cas:106-44-5
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inquiryP-Cresol--99.5% Min CAS No.106-44-5 Appearance: Colorless to yellowish liquid or crystal Purity: 99.5% Min. Appearance:transparent liquid to light yellow liquid Storage:Warehouse ventilation, away from open flame, high temperature, and antio
p-Cresol Product name: p-Cresol English name: p-Cresol Chemical formula: C7H8O CAS No.: 106-44-5 RTECS: 203-398-6 Molar mass: 108.1378 App
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
Cas:106-44-5
Min.Order:1 Metric Ton
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Type:Manufacturers
inquiryOur company was built in 2009 with an ISO certificate.In the past 5 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 on.O
Cas:106-44-5
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inquiryp-Cresol Product name p-Cresol Synonyms 4-Hydroxytoluene; 4-Methylphenol CAS No. 106-44-5 Molecular weight 108.14 Molecular Formula
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Cas:106-44-5
Min.Order:1 Kilogram
FOB Price: $2.0 / 5.0
Type:Trading Company
inquiryHangzhou 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
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:106-44-5
Min.Order:100 Kilogram
Negotiable
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inquiryJ&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
Massive Chemical is certified with ISO9001 and ISO14001 manufacturer for this product. We will offer all documents as requirement for the materials which includes, Certificate of Analysis, Material Safety Data Sheet, and Method of Analysis and
Cas:106-44-5
Min.Order:1 Gram
FOB Price: $1.0
Type:Lab/Research institutions
inquiryZibo 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
Superior quality, moderate price & quick delivery. Appearance:Colorless transparent liquid or crystal Storage:stored in a cool, dry and ventilated place to provent sun and rain Package:25kg/drum Application:the plastics industry in the manufact
We are leading fine chemicals supplier in China with ISO certificate, Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...) 2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...) 3.OLED
Cas:106-44-5
Min.Order:1 Gram
FOB Price: $3.0
Type:Lab/Research institutions
inquiryOur company is engaged in customizing the benzene ring and pyridine derivative organic intermediates, and the quantity is flexible according to customer's needs. It mainly provides high-quality intermediates for domestic and foreign pharmaceuti
Cas:106-44-5
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
inquiryHangzhou 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
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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
Capability on chemical synthesis1. Beijing High-Tech Enterprises2. Strong R&D Team3. 8 years of experiences in R & D of high-tech Catalyst;4. 5000 production techniques, 69 items of national patents, and 360 kinds of products on sales;5. The producti
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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:106-44-5
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
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Conditions | Yield |
---|---|
With ammonium formate; palladium on activated charcoal In methanol for 2h; Ambient temperature; | 100% |
With 20 % Pd(OH)2/C; hydrogen In methanol at 20℃; under 760.051 Torr; for 3h; | 92% |
With kieselguhr; nickel-copper at 453℃; Hydrogenation; | |
With ethanol at 24.84℃; for 48h; Photolysis; Inert atmosphere; | 99 %Chromat. |
With [RuCl2(p-cymene)(P(Fur)3)] In water at 80℃; for 2h; Catalytic behavior; Green chemistry; | >99 %Chromat. |
Conditions | Yield |
---|---|
silica gel; toluene-4-sulfonic acid In water; toluene at 80℃; for 8h; | 100% |
With ammonium acetate In methanol at 20℃; for 4.5h; | 97% |
With mesoporous silica-supported (Salen) Co(II) catalyst In methanol at 20℃; for 1h; chemoselective reaction; | 95% |
4-acetyl-4-methyl-6-phenylselenocyclohex-2-enone
p-cresol
Conditions | Yield |
---|---|
With dihydrogen peroxide In dichloromethane at 0℃; for 2h; | 100% |
4-(tert-butoxy)toluene
p-cresol
Conditions | Yield |
---|---|
With sodium iodide; cerium(III) chloride In acetonitrile at 40℃; for 3h; | 100% |
In methanol at 25℃; Kinetics; Quantum yield; Decomposition; Irradiation; |
Conditions | Yield |
---|---|
With hydrogen In water at 25℃; for 1h; | 99% |
With palladium 10% on activated carbon; water; hydrazine hydrate In ethanol at 100℃; for 24h; Reagent/catalyst; | 99% |
With [(C6H6)(PCy3)(CO)RuH]+*BF4−; hydrogen; phenol In 1,4-dioxane; isopropyl alcohol at 130℃; under 1520.1 Torr; for 12h; Inert atmosphere; Glovebox; Schlenk technique; chemoselective reaction; | 90% |
trimethyl(4-methylphenoxy)silane
p-cresol
Conditions | Yield |
---|---|
With water; bis(benzonitrile)palladium(II) dichloride for 0.05h; desilylation; microwave irradiation; | 99% |
With methanol; 1,3-disulfonic acid imidazolium hydrogen sulfate at 20℃; for 0.0666667h; Green chemistry; | 98% |
With rice husk ash supported on anatase-phase titania nanoparticles nanocomposite In methanol at 20℃; for 0.05h; | 94% |
tert-Butyl(dimethyl)-(4-methylphenoxy)silane
p-cresol
Conditions | Yield |
---|---|
With potassium hydrogen difluoride; 18-crown-6 ether In acetonitrile at 20℃; for 24h; | 99% |
With sodium phosphate dodecahydrate In N,N-dimethyl-formamide at 20℃; for 1.8h; | 97% |
With SO3H silica gel In n-heptane at 50℃; for 0.5h; | 96% |
Conditions | Yield |
---|---|
With oxygen; triethylamine In 2-methyltetrahydrofuran at 20℃; under 760.051 Torr; for 24h; Green chemistry; | 99% |
With water In tetrahydrofuran at 100℃; for 12h; | 99% |
With dihydrogen peroxide at 30℃; for 5h; Green chemistry; | 98% |
1-(methoxymethoxy)-4-methylbenzene
p-cresol
Conditions | Yield |
---|---|
sodium hydrogen sulfate; silica gel In dichloromethane at 20℃; for 1.5h; | 99% |
With tin(IV) chloride In dichloromethane at 0℃; for 0.0333333h; | 95% |
Conditions | Yield |
---|---|
With 2-(N,N-dimethylamino)ethanol; sodium hydroxide; silver(l) oxide In water; dimethyl sulfoxide at 100℃; for 24h; Reagent/catalyst; | 99% |
Stage #1: 4-tolyl iodide With copper(l) iodide; 2-methyl-8-quinolinol; tetra(n-butyl)ammonium hydroxide In water; dimethyl sulfoxide at 100℃; for 7h; Stage #2: With hydrogenchloride In water; N,N-dimethyl-formamide at 20℃; | 97% |
Stage #1: 4-tolyl iodide With copper(l) iodide; 1,10-Phenanthroline; potassium hydroxide In water; dimethyl sulfoxide at 20 - 100℃; Inert atmosphere; Stage #2: With hydrogenchloride In water; dimethyl sulfoxide at 20℃; Inert atmosphere; | 96% |
Conditions | Yield |
---|---|
With palladium dichloride In methanol at 40℃; for 24h; Inert atmosphere; Green chemistry; chemoselective reaction; | A 99% B 99% |
p-Chlor-cinnamyl-p-tolyl-ether
p-cresol
Conditions | Yield |
---|---|
With ethylmagnesium chloride; iron(II) chloride In tetrahydrofuran; m-xylene at 20℃; for 1h; | 99% |
2-(4-methylphenoxy)ethanol
p-cresol
Conditions | Yield |
---|---|
With potassium hydroxide In dimethyl sulfoxide at 100℃; for 3h; Schlenk technique; | 99% |
2-(4-methylphenoxy)tetrahydro-2H-pyran
p-cresol
Conditions | Yield |
---|---|
With methanol at 20℃; for 0.5h; | 98% |
With Montmorillonite KSF In methanol at 40 - 50℃; for 0.4h; | 97% |
With methanol; zirconium(IV) chloride at 20℃; for 2h; | 97% |
allyl p-tolyl ether
p-cresol
Conditions | Yield |
---|---|
With chloro-trimethyl-silane; sodium iodide In acetonitrile for 0.0333333h; | 98% |
With ethylmagnesium chloride; iron(II) chloride In tetrahydrofuran; m-xylene at 20℃; for 1h; | 97% |
With iodine at 20℃; | 92% |
With tetrachlorosilane; borontrifluoride acetic acid; lithium iodide In toluene; acetonitrile at 70℃; for 6h; | 90% |
With 12-TPA/SBA 15 In 1,4-dioxane at 110℃; | 74% |
Conditions | Yield |
---|---|
With ammonium bicarbonate In water at 20℃; for 2h; Schlenk technique; | 98% |
4-(p-tolyloxy)butan-1-ol
p-cresol
Conditions | Yield |
---|---|
With potassium hydroxide In dimethyl sulfoxide at 100℃; for 3h; Schlenk technique; | 98% |
Conditions | Yield |
---|---|
With 1,3-dimethyl-2-imidazolidinone; lithium diisopropyl amide In tetrahydrofuran; n-heptane; ethylbenzene at 185℃; for 12h; further reagent: NaN(SiMe3)2; various temperatures - 65-185 deg C; | 97% |
With N,N,N,N,N,N-hexamethylphosphoric triamide; sodium hydride; N-methylaniline In diethyl ether; xylene at 120℃; for 6.5h; | 95% |
With copper(I) oxide; sodium methylate In methanol at 185℃; for 12h; Autoclave; | 89% |
Conditions | Yield |
---|---|
In water; N,N-dimethyl-formamide at 20℃; for 2.5h; | 97% |
Conditions | Yield |
---|---|
With ammonium chloride; zinc In methanol Heating; | A n/a B 96% |
Conditions | Yield |
---|---|
With Nafion-H; toluene for 2h; Heating; | A 96% B 94 % Chromat. |
2,6-di-tert-butyl-4-methyl-phenol
toluene
A
p-cresol
B
4-tert-butyltoluene
Conditions | Yield |
---|---|
With Nafion-H for 2h; Heating; | A 96% B 94 % Chromat. |
2-thioxo-benzooxazole-3-carboximidic acid p-tolyl ester
A
benzo[d]oxazole-2-(3H)-thione
B
p-cresol
Conditions | Yield |
---|---|
With hydrogenchloride; sodium hydroxide In ethanol for 0.5h; Heating; | A 95% B n/a |
With hydrogenchloride for 7h; Heating; | A 93% B n/a |
3,3-diethyl-1-(4-methylphenyl)-1-triazene
p-cresol
Conditions | Yield |
---|---|
With water; sulfonic acid resin (H+ form) In acetonitrile for 0.166667h; Heating; | 95% |
6,6-bis(4-methylphenyl)-3-methyl-1,2-dioxan-3-ol
A
p-cresol
B
1-[4-(methyl)phenyl]pentane-1,4-dione
Conditions | Yield |
---|---|
With hydrogenchloride In acetic acid at 80℃; for 0.333333h; | A 95% B 67% |
Conditions | Yield |
---|---|
In dichloromethane at 20℃; | 95% |
Conditions | Yield |
---|---|
With dimanganese decacarbonyl In toluene at 20℃; for 6h; Inert atmosphere; Schlenk technique; | A 94% B 95% |
Conditions | Yield |
---|---|
With aluminium trichloride In dichloromethane; ethanethiol at 0℃; for 0.5h; | 94.3% |
With sodium hydroxide; nickel at 150℃; under 7600 Torr; Hydrogenation; |
Conditions | Yield |
---|---|
With copper(I) oxide; tetra(n-butyl)ammonium hydroxide; 1,10-phenanthroline-4,7-diol In water at 110℃; for 24h; Inert atmosphere; Schlenk technique; Sealed tube; Green chemistry; | 94% |
Stage #1: para-bromotoluene With copper(l) iodide; 2-methyl-8-quinolinol; tetra(n-butyl)ammonium hydroxide In water; dimethyl sulfoxide at 130℃; for 21h; Stage #2: With hydrogenchloride In water; N,N-dimethyl-formamide at 20℃; | 93% |
Stage #1: para-bromotoluene With copper(l) iodide; cesium hydroxide; 5-bromo-2-(1H-imidazol-2-yl)pyridine In water; dimethyl sulfoxide; tert-butyl alcohol at 120℃; for 36h; Inert atmosphere; Stage #2: With hydrogenchloride In water; dimethyl sulfoxide; tert-butyl alcohol pH=1 - 2; Inert atmosphere; | 93% |
Conditions | Yield |
---|---|
With hydrogen In water at 20℃; under 7500.75 Torr; for 6h; Autoclave; | 100% |
With nickel(II) oxide; hydrogen; palladium In hexane at 80℃; under 7500.75 Torr; for 10h; | 99% |
With hydrogen; palladium on activated charcoal In hexane at 120℃; under 37503 Torr; Rate constant; var. solvents; |
Conditions | Yield |
---|---|
With hydrogen bromide; acetic acid In dimethyl sulfoxide at 20℃; for 2h; | 100% |
With Oxone; potassium bromide In methanol at 20℃; for 4h; | 99% |
With N-Bromosuccinimide; sulfonic acid functionalized silica In diethyl ether; acetonitrile at 20℃; for 0.166667h; | 99% |
Conditions | Yield |
---|---|
With (NH4)2Ce(NO3)6 supported on pillared bentonite In water at 25℃; for 48h; | 100% |
With chloro-trimethyl-silane; copper(ll) sulfate pentahydrate; guanidine nitrate In acetonitrile at 20℃; | 99% |
With silica-acetate; dinitrogen tetraoxide In ethyl acetate for 0.333333h; Heating; | 95% |
Conditions | Yield |
---|---|
With pyridine at 100℃; for 15h; | 100% |
at 20℃; for 0.666667h; | 100% |
With pyridine at 25℃; for 12h; | 100% |
p-cresol
1-bromomethyl-4-nitro-benzene
4-methylphenyl 4-nitrobenzyl ether
Conditions | Yield |
---|---|
With sodium hydroxide In water for 0.00277778h; microwave irradiation; | 100% |
With sodium hydroxide; Aliquat 360 In dichloromethane; water at 25℃; for 24h; | 89% |
With potassium carbonate; acetone | |
With alkaline solution |
Conditions | Yield |
---|---|
erbium(III) triflate In acetonitrile at 20℃; for 8h; | 100% |
at 100℃; Cooling with ice; | 93% |
p-cresol
3,5-dinitrobenoyl chloride
3,5-dinitrobenzoate of 4-methylphenol
Conditions | Yield |
---|---|
With pyridine In tetrahydrofuran for 0.333333h; Heating; | 100% |
With pyridine | |
Stage #1: p-cresol With base Stage #2: 3,5-dinitrobenoyl chloride phase transfer; Further stages.; |
Conditions | Yield |
---|---|
With triethylamine In ethyl acetate at 0 - 20℃; for 0.166667h; Green chemistry; | 100% |
With pyridine In dichloromethane at 0 - 20℃; Inert atmosphere; | 91% |
With pyridine In dichloromethane at 0 - 20℃; Inert atmosphere; | 80% |
Conditions | Yield |
---|---|
With potassium carbonate In acetone Reflux; | 100% |
Stage #1: p-cresol With potassium carbonate In N,N-dimethyl-formamide for 0.166667h; Schlenk technique; Inert atmosphere; Stage #2: propargyl bromide In N,N-dimethyl-formamide at 20℃; for 24h; Schlenk technique; Inert atmosphere; | 99% |
With caesium carbonate In acetonitrile | 93% |
p-cresol
Bromoacetaldehyde diethyl acetal
1-(2,2-diethoxyethoxy)-4-methylbenzene
Conditions | Yield |
---|---|
Stage #1: p-cresol With sodium hydride In N,N-dimethyl-formamide; mineral oil at 0 - 20℃; for 0.5h; Stage #2: Bromoacetaldehyde diethyl acetal In N,N-dimethyl-formamide; mineral oil Reflux; | 100% |
Stage #1: p-cresol With sodium hydride In N,N-dimethyl-formamide at 0℃; for 0.166667h; Inert atmosphere; Stage #2: Bromoacetaldehyde diethyl acetal In N,N-dimethyl-formamide at 120℃; for 6h; Inert atmosphere; | 98% |
With potassium hydroxide In N,N-dimethyl acetamide at 20℃; Heating; | 96% |
Conditions | Yield |
---|---|
With perchloric acid; d(4)-methanol at 75℃; for 144h; Inert atmosphere; | 100% |
With water-d2; phosphorus tribromide for 5h; Yield given; | |
With water-d2; phosphorus tribromide Reflux; |
p-cresol
tert-butyldimethylsilyl chloride
tert-Butyl(dimethyl)-(4-methylphenoxy)silane
Conditions | Yield |
---|---|
With 1H-imidazole In N,N-dimethyl-formamide | 100% |
With 1H-imidazole In N,N-dimethyl-formamide at 20℃; for 16h; | 99% |
With 1H-imidazole; 3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate at 20℃; for 2h; | 97% |
Conditions | Yield |
---|---|
With potassium carbonate In butanone for 5.5h; Heating; | 100% |
With caesium carbonate In N,N-dimethyl-formamide at 20℃; for 3h; | 90% |
With caesium carbonate In N,N-dimethyl-formamide at 20℃; for 3h; | 90% |
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 18h; | 85% |
With potassium carbonate In tetrahydrofuran at 20 - 80℃; |
Conditions | Yield |
---|---|
100% | |
at 20 - 160℃; for 2h; Inert atmosphere; |
Conditions | Yield |
---|---|
With sodium hydride In N,N-dimethyl-formamide at 20℃; for 26h; | 100% |
Stage #1: p-cresol With sodium hydride In N,N-dimethyl-formamide; paraffin oil at 0 - 20℃; for 1h; Stage #2: chloromethyl methyl ether In N,N-dimethyl-formamide; paraffin oil at 20℃; for 24h; | 100% |
(i) NaH, DMF, (ii) /BRN= 505943/; Multistep reaction; |
p-cresol
2-chloro-2,2-difluoroacetic acid
difluoro-(4-methylphenoxy)acetic acid
Conditions | Yield |
---|---|
With sodium hydride In 1,4-dioxane for 3h; Heating; | 100% |
Conditions | Yield |
---|---|
With potassium carbonate In acetone at 50℃; | 100% |
Stage #1: p-cresol With potassium carbonate In N,N-dimethyl-formamide for 0.166667h; Stage #2: 2-Iodobenzyl bromide In N,N-dimethyl-formamide at 20℃; | 62% |
Stage #1: p-cresol With sodium hydride In tetrahydrofuran for 0.5h; Metallation; Heating; Stage #2: 2-Iodobenzyl bromide In tetrahydrofuran for 4h; Etherification; Heating; Further stages.; | 40% |
p-cresol
di-tert-butyl dicarbonate
1-(tert-butoxycarbonyloxy)-4-methylbenzene
Conditions | Yield |
---|---|
With dmap In acetonitrile at 20℃; for 0.25h; Product distribution; Further Variations:; Reagents; reaction time; Condensation; | 100% |
With mesoporous silica MCM-41 supported erbium(III) at 40℃; for 1.5h; Neat (no solvent); ultrasound irradiation; Inert atmosphere; | 99% |
With MgO-ZrO2 nanoparticle at 60℃; for 1.5h; neat (no solvent); chemoselective reaction; | 92% |
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 98℃; for 3h; | 100% |
With potassium carbonate In N,N-dimethyl-formamide |
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 98℃; for 3h; | 100% |
With potassium carbonate In N,N-dimethyl-formamide |
p-cresol
1,1,1,2,2,2-hexamethyldisilane
trimethyl(4-methylphenoxy)silane
Conditions | Yield |
---|---|
In pyridine at 115℃; for 3h; | 100% |
With lanthanum(III) nitrate hexahydrate In acetonitrile at 20℃; | 90% |
Conditions | Yield |
---|---|
In dichloromethane under Ar: addn. of CF3SO3H to a stirred dichloromethane soln. of ((C5(CH3)5)RuOCH3)2; stirring for 15 min at room temperature; addn. of a soln. of p-cresol in dichloromethane; stirring for 2 h;; removing of the solvent; crystallization from dichloromethane/diethyl ether; elem. anal.; | 100% |
Conditions | Yield |
---|---|
In benzene addn. of p-cresol to the Ge compd. in benzene (inert gas) and heating at 120°C for 2 h; evapn. (vac.); elem. anal.;; | 100% |
In neat (no solvent) addn. of p-cresol to the Ge compd. in a Schlenk tube (inert gas) and heating at 166-195°C for ca. 1 h; evapn. (vac.); elem. anal.;; | |
In not given byproducts: NH3; |
p-cresol
tetramethyl-diphosphine disulphide
A
dimethylphosphine sulfide
B
O-(p-tolyl) dimethylphosphinothioate
Conditions | Yield |
---|---|
With hydridotetakis(triphenylphosphine)rhodium(I); 1,2-bis(dimethylphosphanyl)ethane In tetrahydrofuran for 3h; Inert atmosphere; Reflux; | A n/a B 100% |
p-cresol
2,4-dinitrophenyl benzoate
A
p-cresyl benzoate
B
potassium 2,4-dinitrophenolate
Conditions | Yield |
---|---|
With potassium hydrogencarbonate In N,N-dimethyl-formamide at 25℃; for 5h; | A 100% B n/a |
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