Multi-target purpose intermediate with wide usage Commercial production from grams to tons, with technical documents package support, and audit and inspection support. With high purity and optimized and stable process. Self Innovation Appe
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
Cas:767-00-0
Min.Order:1 Kilogram
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Type:Lab/Research institutions
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Min.Order:0 Metric Ton
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Type:Manufacturers
inquiryItems Standard Result Appearance White flake-like crystal or powder Complies Assay(%) 99.5%
Cas:767-00-0
Min.Order:1 Gram
FOB Price: $100.0 / 500.0
Type:Manufacturers
inquiryProduct description: Product name 4-Cyanophenol CAS number 767-00-0 Assay >95% Appearance White needle-like crystals or light yellow crystals or crystalline powder Capacity 100mt/year
Cas:767-00-0
Min.Order:10 Gram
FOB Price: $12.0
Type:Lab/Research institutions
inquiryhe 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 se T rvice Appearance:Whit
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
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Cas:767-00-0
Min.Order:1 Gram
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Type:Manufacturers
inquiryCangzhou Enke Pharma Tech Co.,ltd. is located in Cangzhou City, Hebei province ,where is a famous petroleum chemical industry city in China. Enke Pharma a high-tech enterprise ,and we are dedicated to developing and manufacturing new ap
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Min.Order:1 Metric Ton
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inquiryOur 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
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Type:Manufacturers
inquiryLIDE PHARMACEUTICALS LIMITED is a professional chemicals and APIs leading manufacturer in China. Our core business line covers APIs, Intermediates, Herb extract, etc. We are specialized in chemical synthesis, process development of pharmaceu
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Min.Order:1 Kilogram
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inquiry4-Cyanophenol Basic information Product Name: 4-Cyanophenol Synonyms: 4-Cyanolphenol;4-hydroxy-benzonitril;Benzonitrile, 4-hydroxy-;Benzonitrile, p-hydroxy-;Benzoni
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Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
inquiryWith our good experience, we offer detailed technical support and advice to assist customers. We communicate closely with customers to establish their quality requirements. Consistent Quality Our plant has strict quality control in each manufactu
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Min.Order:1 Kilogram
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inquiryName: 4-Cyanophenol CAS:767-00-0 MF: C7H5NO Appearance:White Powder Storage:Store in cool and dry place, away from sun light. Package:25kg Application:Pharmaceutical intermediate;Agrochemical Intermediates Transportation:By sea or by air Port:Qin
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Min.Order:10 Kilogram
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inquiry4-Cyanophenol CAS:767-00-0 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic intermediates
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Min.Order:1 Gram
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Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
inquiryHenan 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
Company information: Hebei Mojin Biotechnology Co., Ltd, Our company is a professional in chemical raw materials and chemical reagents research and development production enterprises. Our business covers more than 30 countries, most of the big custo
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Min.Order:1 Kilogram
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Company Introduction 1. Established in 2005, with two independent business divisions: Fine chemicals division; Pharmaceutical division. 2. Main product: Optical brightener Textile auxiliary Dye stuff Pigments
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
4-cyanophenyl acetate
4-cyanophenol
Conditions | Yield |
---|---|
With 1-methyl-pyrrolidin-2-one; potassium carbonate; thiophenol for 0.25h; Hydrolysis; Heating; | 100% |
With potassium hydroxide In ethanol for 0.333333h; Heating; | 88% |
With sodium tetrahydroborate; cobalt(II) chloride In ethanol at 0 - 25℃; for 10h; | 83% |
With N-butylamine; Tetraethylene glycol dimethyl ether In chlorobenzene at 25℃; Rate constant; efficacy of glyme catalysis, other glymes; |
Conditions | Yield |
---|---|
With 1-methyl-pyrrolidin-2-one; hydroxylamine hydrochloride at 100℃; for 0.25h; Condensation; microwave irradiation; | 100% |
With oxygen; copper; ammonium chloride In pyridine at 60℃; for 24h; | 99% |
With sodium azide; trifluorormethanesulfonic acid In acetonitrile at 20℃; for 0.0333333h; Schmidt reaction; | 99% |
Conditions | Yield |
---|---|
With calcium hydride; diphenyldisulfane In 1-methyl-pyrrolidin-2-one at 220℃; for 0.5h; | 100% |
With sodium methylate; 1-dodecylthiol In N,N-dimethyl-formamide at 100℃; for 1h; | 97% |
With cyclohexa-1,4-diene; 3,6-bis(dimethylamino)-9H-carbazole; caesium carbonate In dimethyl sulfoxide at 23℃; for 48h; Inert atmosphere; Schlenk technique; Irradiation; | 94% |
4-allyloxy-benzonitrile
4-cyanophenol
Conditions | Yield |
---|---|
With calcium hydride; diphenyldisulfane In 1-methyl-pyrrolidin-2-one at 220℃; for 0.5h; | 100% |
With tetrabutylammonium tetrafluoroborate; tris(2,2'-bipyridine)nickel(II) tetrafluoroborate In N,N-dimethyl-formamide Ambient temperature; electrolysis: Mg rod anode, carbon fibre cathode, const. current 60 mA; | 99% |
With aniline; (ϖ-allyl)palladium triflate based catalyst at 30℃; for 0.333333h; | 99% |
(E)-4-hydroxybenzaldehyde oxime
4-cyanophenol
Conditions | Yield |
---|---|
With 1,3,5-trichloro-2,4,6-triazine In N,N-dimethyl-formamide at 20℃; for 4h; Beckmann rearrangement; | 100% |
With [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; 4 A molecular sieve In acetonitrile at 80℃; for 0.5h; | 99% |
for 0.0583333h; Dehydration; Irradiation; | 82% |
4-cyanophenyl benzoate
4-cyanophenol
Conditions | Yield |
---|---|
With 1-methyl-pyrrolidin-2-one; potassium carbonate; thiophenol for 0.25h; Hydrolysis; debenzoylation; Heating; | 100% |
With potassium fluoride; thiophenol In 1-methyl-pyrrolidin-2-one at 100℃; for 1h; | 85% |
With sodium; diphenyldisulfane In 1-methyl-pyrrolidin-2-one at 90℃; for 0.25h; | 84% |
With potassium carbonate In 1-methyl-pyrrolidin-2-one for 0.333333h; Heating; | 80% |
4-cyanophenyl acetate
2-amino-benzenethiol
A
2-Methylbenzothiazole
B
4-cyanophenol
Conditions | Yield |
---|---|
With 1-methyl-pyrrolidin-2-one; potassium carbonate at 100℃; for 0.5h; Hydrolysis; cyclization; | A n/a B 100% |
2-amino-benzenethiol
4-cyanophenyl pivalate
A
2-(tert-butyl)benzo[d]thiazole
B
4-cyanophenol
Conditions | Yield |
---|---|
With 1-methyl-pyrrolidin-2-one; potassium carbonate at 100℃; for 1.5h; Hydrolysis; cyclization; | A n/a B 100% |
4-benzyloxybenzonitrile
4-cyanophenol
Conditions | Yield |
---|---|
With calcium hydride; diphenyldisulfane In 1-methyl-pyrrolidin-2-one at 220℃; for 0.5h; | 100% |
With hydrogen; palladium on activated charcoal; ethylenediamine In tetrahydrofuran at 20℃; for 24h; atmospheric pressure; | 100% |
With cyclohexa-1,4-diene; 3,6-bis(dimethylamino)-9H-carbazole; caesium carbonate In dimethyl sulfoxide at 23℃; for 18h; Inert atmosphere; Schlenk technique; Irradiation; | 99% |
Conditions | Yield |
---|---|
With nickel dibromide In 1-methyl-pyrrolidin-2-one at 200℃; under 10343 Torr; for 0.333333h; microwave irradiation; | 99% |
Conditions | Yield |
---|---|
With tetrabutylammomium bromide In water at 170℃; under 10343.2 Torr; for 0.0833333h; microwave irradiation; | 99% |
Conditions | Yield |
---|---|
With β-D-glucose; copper(II) acetate monohydrate; potassium hydroxide In water; dimethyl sulfoxide at 20 - 120℃; for 28h; | 99% |
With bis(η3-allyl-μ-chloropalladium(II)); p-methylbenzaldehyde oxime; caesium carbonate; tert-butyl XPhos In tetrahydrofuran at 75℃; for 2h; Inert atmosphere; | 98% |
With cesiumhydroxide monohydrate; t-BuBrettPhos; C44H62NO5PPdS; water In 1,4-dioxane at 20℃; for 18h; Inert atmosphere; | 97% |
4-cyanophenylboronic acid
4-cyanophenol
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In water; acetonitrile for 30h; Irradiation; | 99% |
With oxygen; triethylamine In acetonitrile at 20℃; under 760.051 Torr; for 4h; Reagent/catalyst; Irradiation; | 99% |
With water; caesium carbonate; hydrazine hydrate at 80℃; for 12h; | 98% |
4-(dimethylsilyl)benzonitrile
4-cyanophenol
Conditions | Yield |
---|---|
With water; dihydrogen peroxide; potassium hydrogencarbonate In tetrahydrofuran; methanol at 20℃; for 5h; | 99% |
Multi-step reaction with 2 steps 1: (p-cymene)ruthenium(II) chloride / 0.08 h / 20 °C 2: tetrabutyl ammonium fluoride; water; dihydrogen peroxide; potassium hydrogencarbonate / tetrahydrofuran; methanol / 0.5 h / 20 °C View Scheme | |
With dihydrogen peroxide; potassium hydrogencarbonate In tetrahydrofuran-d8; d(4)-methanol at 20℃; Kinetics; Mechanism; |
Conditions | Yield |
---|---|
With 0.5%Pd/TiO2; isopropyl alcohol In water at 24.84℃; for 2h; Inert atmosphere; Sealed tube; Irradiation; | A 99% B 99% |
Conditions | Yield |
---|---|
With phosphorus pentoxide; urea at 160℃; for 1h; Temperature; | 98.2% |
With hydroxyammonium sulfate; zinc for 0.316667h; Microwave irradiation; | 91% |
With phosphoramide; sodium chloride at 450℃; for 1.5h; | 68% |
Multi-step reaction with 2 steps 1: ammonia / 0.5 h / 250 °C 2: 1 h / 325 °C View Scheme | |
Multi-step reaction with 3 steps 1: sulfuric acid / cyclohexane / 10 h / 90 °C 2: ammonium hydroxide / 5 h / 100 °C / Autoclave 3: resin catalyst supported with palladium salt / water; acetonitrile / 7 h / 50 °C View Scheme |
4-hydroxybenzaldehyde oxime
4-cyanophenol
Conditions | Yield |
---|---|
With thionyl chloride; sodium sulfite at 0℃; for 0.0166667h; | 98% |
With thionyl chloride; silica gel In dichloromethane at 0℃; for 0.116667h; | 98% |
With acetonitrile for 1h; Reflux; Green chemistry; | 98% |
potassium (4-cyanophenyl)trifluoroborate
4-cyanophenol
Conditions | Yield |
---|---|
With Oxone; water In acetone at 20℃; for 0.0333333h; | 98% |
Conditions | Yield |
---|---|
With copper (II) trifluoroacetate hydrate; palladium diacetate In dimethyl sulfoxide at 130℃; for 6h; Sealed tube; Inert atmosphere; | 98% |
Conditions | Yield |
---|---|
With ammonium bicarbonate In water at 20℃; for 2h; Schlenk technique; | 97% |
Conditions | Yield |
---|---|
With diethylenetriaminopentaacetic acid In aq. phosphate buffer; acetonitrile at 37℃; pH=7.4; | A n/a B 97% |
Conditions | Yield |
---|---|
With ammonia; boron phosphate at 400℃; for 0.000277778h; | A 96% B 5% |
A 95% B n/a | |
A 93.8% by weight. B n/a |
Conditions | Yield |
---|---|
With resin catalyst supported with palladium salt In water; acetonitrile at 50℃; for 7h; Temperature; | 96% |
With trichloromethyl chloroformate In various solvent(s) 0-5 deg C then heated to 60 deg C, 5 min; | 94% |
Stage #1: p-hydroxybenzamide With C39H45N2 In acetonitrile at 20℃; Schlenk technique; Glovebox; Inert atmosphere; Stage #2: With phenylsilane In acetonitrile at 20℃; for 12h; Schlenk technique; Inert atmosphere; Sealed tube; | 94% |
4-cyanophenyl propyl ether
4-cyanophenol
Conditions | Yield |
---|---|
With 1-n-butyl-3-methylimidazolim bromide at 200 - 220℃; for 0.5h; Microwave irradiation; Inert atmosphere; | 96% |
With tetrabutylammonium tetrafluoroborate In N,N-dimethyl-formamide at 20℃; Kinetics; Electrolysis; |
Conditions | Yield |
---|---|
With trichloroisocyanuric acid; ammonia In water at 20 - 60℃; | 96% |
With potassium hydroxide; ammonium bicarbonate; (Bu4N)2S2O8; copper(II) formate; nikel(II) formate In isopropyl alcohol at 25℃; for 1.5h; | 91% |
With ammonia; oxygen In 1,4-dioxane for 2.5h; Reflux; | 91% |
Conditions | Yield |
---|---|
With ammonia; boron phosphate at 400℃; for 0.00111111h; | A 95% B 5% |
Conditions | Yield |
---|---|
With 2-(methylsulfonyl)ethyl alcohol; sodium hydride In N,N-dimethyl-formamide at 0 - 20℃; | 95% |
With acetylhydroxamic acid; potassium carbonate In dimethyl sulfoxide at 80℃; for 16h; Sealed tube; | 93% |
With methyl propargyl alcohol; potassium tert-butylate In dimethyl sulfoxide at 125℃; for 0.0333333h; microwave irradiation; | 90% |
4-(tert-butoxycarbonyloxy)benzonitrile
4-cyanophenol
Conditions | Yield |
---|---|
With methanol; carbon tetrabromide; triphenylphosphine for 1h; Reflux; | 95% |
Conditions | Yield |
---|---|
With tris(6,6'-diamino-2,2'-bipyridine); 4,4-diphenyl-1,3,5,7,8-pentamethyl-2,6-diethyl-4-bora-3a,4a-diaza-s-indacene; Br2Ni*3H2O; water; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide; acetonitrile at 20℃; for 24h; Glovebox; Irradiation; Inert atmosphere; | 95% |
With dicyclohexyl-(2′,4′,6′-triisopropyl-3,6-dimethoxy-[1,1′-biphenyl]-2-yl)phosphine; boric acid; palladium diacetate; caesium carbonate In 1-methyl-pyrrolidin-2-one at 80℃; for 24h; Schlenk technique; Inert atmosphere; | 95% |
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; | 88% |
Conditions | Yield |
---|---|
With oxygen; copper(II) trifluoroacetate; urea In dimethyl sulfoxide at 95℃; for 16h; Green chemistry; | 95% |
With 1,10-Phenanthroline; oxygen; copper(II) oxide; potassium ferrocyanide In dimethyl sulfoxide at 120℃; under 11251.1 Torr; for 40h; Autoclave; | 36% |
Conditions | Yield |
---|---|
With caesium carbonate In water; N,N-dimethyl-formamide at 20℃; for 12h; | 100% |
With potassium carbonate In acetone at 20℃; for 24h; | 99% |
With potassium carbonate In acetone at 20℃; for 20h; Reflux; | 98% |
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 |
---|---|
With magnesium(II) perchlorate at 80℃; for 0.25h; | 100% |
With thalium(III) chloride tetrahydrate at 20℃; for 0.0333333h; | 97% |
With aluminum triflate at 20℃; for 0.00833333h; | 96% |
Conditions | Yield |
---|---|
With sodium carbonate In acetone for 16h; Reflux; | 100% |
With potassium carbonate In acetone for 5h; Heating; | 98% |
With potassium carbonate In acetone Reflux; | 98% |
Conditions | Yield |
---|---|
With sodium In ethanol for 24h; Heating; | 100% |
With potassium carbonate In acetone Reflux; | 100% |
trifluoromethylsulfonic anhydride
4-cyanophenol
4-cyanophenyl trifluoromethanesulfonate
Conditions | Yield |
---|---|
With 2,6-dimethylpyridine In dichloromethane at 20℃; for 16h; | 100% |
With pyridine In dichloromethane at 20℃; for 1h; | 96% |
With potassium phosphate In water; toluene at 0 - 20℃; | 96% |
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 0 - 20℃; for 12h; | 100% |
In benzene Heating; | |
With pyridine In diethyl ether | |
With triethylamine In dichloromethane at 0 - 5℃; |
Conditions | Yield |
---|---|
With cesium fluoride/clinoptilolite In dimethyl sulfoxide at 110℃; for 0.5h; Ullmann Condensation; | 100% |
With potassium carbonate In N,N-dimethyl-formamide at 100℃; for 24h; | 99% |
With potassium hydroxide In dimethyl sulfoxide at 55℃; | 98% |
Conditions | Yield |
---|---|
In potassium carbonate | 100% |
With sodium hydride In N,N-dimethyl-formamide 1.) rt, 1 h, 2.) reflux, 12 h; | 90% |
With potassium carbonate In cyclohexanone for 24h; Heating; | 70% |
Conditions | Yield |
---|---|
With magnesium(II) perchlorate at 80℃; for 0.75h; | 100% |
With potassium tropolonato In acetonitrile at 70℃; for 4h; | 80% |
Conditions | Yield |
---|---|
With bis-(2-(1-adamantyl)ethyl) azodicarboxylate; triphenylphosphine Mitsunobu reaction; | 100% |
ethyl 2-bromoisobutyrate
4-cyanophenol
2-(4-cyanophenoxy)-2-methylpropionic acid ethyl ester
Conditions | Yield |
---|---|
Stage #1: 4-cyanophenol With potassium carbonate In acetonitrile for 1h; Heating / reflux; Stage #2: ethyl 2-bromoisobutyrate With potassium carbonate for 72h; Heating / reflux; | 100% |
Stage #1: 4-cyanophenol With potassium carbonate In N,N-dimethyl-formamide for 0.166667h; Stage #2: ethyl 2-bromoisobutyrate In N,N-dimethyl-formamide at 20℃; for 16h; | 69% |
Stage #1: 4-cyanophenol With potassium carbonate In acetone at 20℃; for 0.5h; Stage #2: ethyl 2-bromoisobutyrate In acetone for 16h; Heating / reflux; | 46.9% |
Conditions | Yield |
---|---|
With potassium carbonate In acetone; toluene for 24h; Williamson Ether Synthesis; Reflux; | 100% |
Stage #1: 4-cyanophenol With potassium carbonate In N,N-dimethyl-formamide at 80℃; for 0.5h; Stage #2: propargyl bromide In N,N-dimethyl-formamide; toluene at 80℃; for 15h; | 97% |
With potassium carbonate In N,N-dimethyl-formamide at 50℃; for 5h; Inert atmosphere; | 95% |
(2,2,8-trimethyl-4H-[1,3]dioxino[4,5-c]pyridin-5-yl)methanol
4-cyanophenol
4-(2,2,8-trimethyl-4H-[1,3]dioxino[4,5-c]pyridin-5-ylmethoxy)-benzonitrile
Conditions | Yield |
---|---|
With triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran at 20℃; for 1.5h; | 100% |
4-cyanophenol
bromoacetic acid methyl ester
methyl 2-(4-cyanophenoxy)acetate
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 70℃; for 1.5h; | 100% |
With potassium carbonate In acetonitrile at 20℃; |
di-tert-butyl dicarbonate
4-cyanophenol
4-(tert-butoxycarbonyloxy)benzonitrile
Conditions | Yield |
---|---|
With 6,7-dimethoxyisoquinoline In dichloromethane at 20℃; for 10h; Inert atmosphere; chemoselective reaction; | 100% |
Stage #1: 4-cyanophenol With dmap; triethylamine In dichloromethane for 0.25h; Stage #2: di-tert-butyl dicarbonate In dichloromethane for 2h; | 100% |
triphenylphosphine at 40℃; for 14h; | 97% |
4-cyanophenol
2,4-dinitrophenyl benzoate
A
4-cyanophenyl 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 |
4-cyanophenol
2-bromobutyric acid ethyl ester
Ethyl 2-(4-cyanophenoxy)butanoate
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 80℃; for 3h; | 100% |
With potassium carbonate In acetonitrile at 80℃; for 3h; | 100% |
Conditions | Yield |
---|---|
With potassium iodide In N,N-dimethyl-formamide at 60℃; for 10h; Reagent/catalyst; Solvent; Temperature; | 100% |
With potassium carbonate; potassium iodide In N,N-dimethyl-formamide at 80℃; for 6h; | 98.5% |
With tetra-(n-butyl)ammonium iodide In N,N-dimethyl-formamide at 70℃; for 18h; | 98% |
Conditions | Yield |
---|---|
With C45H65FeNO3P2PdS; caesium carbonate In toluene at 100℃; for 24h; Inert atmosphere; Sealed tube; | 100% |
Conditions | Yield |
---|---|
With potassium carbonate In acetone for 4h; Reflux; | 100% |
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