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
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inquiryProduct Description Product website: http://www.finerchem.com Product Name 5-Amino-o-cresol CAS No. 2835-95-
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inquiry5-Amino-o-cresol CAS 2835-95-2 Company profile Wuhan Fortuna Chemical Co.,Ltd established in 2006, is a big integrative chemical enterprise being engaged in Pharmaceutical & its intermediates, Food/Feed additives, Fine chemicals in distribut
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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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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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inquiryAbout Product Details
Cas:2835-95-2
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inquiry5-Amino-o-cresol Basic information Product Name: 5-Amino-o-cresol Synonyms: JAROCOL 2M5AP;3-HYDROXY-4-METHYLANILINE;4-AMINO-2-HYDROXYTOLUENE;5-AMINO-2-METHYLPHENOL;5-AMINO-O-CRESOL;2-Hyd
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inquiryOur advantages: 1. All inquiries will be replied within 12 hours. 2. Dedication to quality, supply & service. 3. Strictly on selecting raw materials. 4. Reasonable & competitive price, fast lead time. 5. Sample is available for your eva
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inquiryWITH US,YOUR MONEY IN SAFE,YOUR BUSINESS IN SAFE 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 et
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inquiryProduct Name 4-Amino-o-cresol Synonyms 4-Amino-2-methylphenol CAS Registry Number 2835-96-3 Molecular Structure
Cas:2835-95-2
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inquiryAppearance:Yellow crystal Storage:R.T Package:25kg/drum Application:Pharmaceutical intermediates Transportation:Express/Sea/Air Port:Any port in China
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inquiry2835-95-2 CAS 5-Amino-o-cresol 2-Methyl-5-Amino-Phenol Packing: According to customer requirements Delivery time: In stock or depands Port of shipment: Ningbo/Shanghai/Qingdao OEM/ODM:Welcome Sample:We can offer our existing samples at once A
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inquiry5-Amino-o-cresolCAS:2835-95-2 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 intermedia
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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
5-Amino-o-cresol CAS: 2835-95-2 Specificatio Product Name 5-Amino-o-cresol CAS No. 2835-95-2 Appearance Beige crystal Assay ≥99%
Cas:2835-95-2
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inquiryHangzhou Fanda Chemical Co.,Ltd (FandaChem) , a China-based chemical company, specialize in exporting 5-Amino-o-cresol (5-Amino Ortho Cresol),cas 2835-95-2 from FandaChem, Please contact us by email freely. We are leading exporter in China.
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inquiry1,we produce and sell good chemicals around the world. 2,our success rate is about 95%. this means, if customer order is accepted, the probability that the customer will obtain the ordered substances, is 95%. 3,our staff consists of highly qualifie
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inquiry5-Amino-o-cresol CAS 2835-95-2 Purity: 99% Min Application: Intermediates Appearance: Powder Package: Bag Delivery: 3-5days Our Advantage & Service 1.Top quality: Using high quality material and establishing a strict quality control
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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
5-Amino-o-cresol CAS 2835-95-2 Our advantage 1.Top quality: Using high quality material and establishing a strict quality control system,assigning specific persons in charge of each part of production,from raw material purchase to assembly.
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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
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inquiryConditions | Yield |
---|---|
With copper; copper(l) chloride; sodium hydroxide In ethanol at 175℃; for 4h; Reagent/catalyst; Autoclave; Inert atmosphere; Industrial scale; | 85.36% |
Conditions | Yield |
---|---|
With dihydrogen peroxide; antimony pentafluoride In hydrogen fluoride at -20℃; for 0.25h; Mechanism; Product distribution; | 71% |
With dihydrogen peroxide; antimony pentafluoride In hydrogen fluoride at -20℃; for 0.25h; | 71% |
N-(4-dimethylaminomethyl-3-hydroxyphenyl)acetamide
amino-4 hydroxy-2 toluene
Conditions | Yield |
---|---|
palladium on activated carbon In potassium hydroxide | 68% |
Conditions | Yield |
---|---|
With hydrogenchloride; tin | |
With palladium on activated charcoal; ethyl acetate Hydrogenation; | |
With sodium hydroxide; sodium dithionite |
Conditions | Yield |
---|---|
With hydrogenchloride |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: sodium nitrite; hydrochloric acid / anschliessend Verkochen 2: hydrochloric acid View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: sulfuric acid; HNO3+H2SO4 / Verseifung der Acetylverbindung 2: concentrated sulfuric acid; water; NaNO2 / Diazotization 3: tin; hydrochloric acid View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: sulfuric acid; nitric acid 2: concentrated sulfuric acid; water; NaNO2 / Diazotization 3: tin; hydrochloric acid View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: concentrated sulfuric acid; water; NaNO2 / Diazotization 2: tin; hydrochloric acid View Scheme | |
Multi-step reaction with 2 steps 1: (i) aq. NaNO2, H2SO4, (ii) aq. H2SO4 2: N2H4*H2O / Raney-Ni View Scheme |
amino-4 hydroxy-2 toluene
4-chloro-benzoyl chloride
4-chloro-benzoic acid 5-(4-chloro-benzoylamino)-2-methyl-phenyl ester
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 0 - 20℃; for 16h; | 100% |
amino-4 hydroxy-2 toluene
m-Chlorobenzoyl chloride
3-chloro-benzoic acid 5-(3-chloro-benzoylamino)-2-methyl-phenyl ester
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 0 - 20℃; for 16h; | 100% |
With triethylamine In tetrahydrofuran at 20℃; for 16h; |
amino-4 hydroxy-2 toluene
3-chloro-4-fluorobenzoyl chloride
3-Chloro-4-fluoro-benzoic acid 5-(3-chloro-4-fluoro-benzoylamino)-2-methyl-phenyl ester
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 0 - 20℃; for 16h; | 100% |
With triethylamine In tetrahydrofuran at 20℃; for 16h; | |
With triethylamine In tetrahydrofuran at 20℃; for 16h; |
potassium cyanate
amino-4 hydroxy-2 toluene
3-hydroxy-4-methyl-phenyl urea
Conditions | Yield |
---|---|
With acetic acid In water at 35℃; for 24h; | 99% |
amino-4 hydroxy-2 toluene
4-chloro-7-methoxy-quinoline-3-carbonitrile
Conditions | Yield |
---|---|
With pyridine hydrochloride In 2-ethoxy-ethanol for 1h; Heating / reflux; | 99% |
With pyridine hydrochloride In 2-ethoxy-ethanol; water | 277 mg (99%) |
With pyridine hydrochloride In 2-ethoxy-ethanol; water | 277 mg (99 %) |
amino-4 hydroxy-2 toluene
2-(7-hydroxy-5,8-dimethyl-1,2,3,4-tetrahydronapthalen-2-yl)propanoic acid
Conditions | Yield |
---|---|
Stage #1: 2-(7-hydroxy-5,8-dimethyl-1,2,3,4-tetrahydronapthalen-2-yl)propanoic acid With thionyl chloride In benzene Reflux; Stage #2: amino-4 hydroxy-2 toluene With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃; for 6h; | 98% |
amino-4 hydroxy-2 toluene
4-amino-phenol
N-<-(4'-Hydroxy)-phenyl>-3-amino-6-methyl-benzochinon
Conditions | Yield |
---|---|
With CotA-laccase from Bacillus subtilis; oxygen In aq. phosphate buffer; ethanol at 37℃; for 24h; pH=7; Green chemistry; Enzymatic reaction; | 98% |
amino-4 hydroxy-2 toluene
5-amino-4-iodo-2-methylphenol
Conditions | Yield |
---|---|
With hydrogenchloride; potassium iodate; potassium iodide In water at 0 - 25℃; for 1h; | 97% |
With [K(18-crown-6)]ICl2; calcium carbonate In acetonitrile at 50℃; for 4h; regioselective reaction; | 62% |
amino-4 hydroxy-2 toluene
pivaloyl chloride
N-(3-hydroxy-4-methylphenyl)-2,2-dimethylpropionamide
Conditions | Yield |
---|---|
With sodium carbonate In water; ethyl acetate at 20℃; for 1h; | 97% |
With sodium hydrogencarbonate In water at 0 - 20℃; | 96% |
Inert atmosphere; Schlenk technique; Alkaline conditions; |
2,4-dimethylaniline-5-sulfonic acid
amino-4 hydroxy-2 toluene
(E)-5-((2-amino-4-hydroxy-5-methylphenyl)diazenyl)-2,4-dimethylbenzenesulfonic acid
Conditions | Yield |
---|---|
Stage #1: 2,4-dimethylaniline-5-sulfonic acid With hydrogenchloride; sodium nitrite at 0℃; for 2h; Stage #2: amino-4 hydroxy-2 toluene With sodium hydroxide In water at 0℃; for 1h; pH=8 - 10; Inert atmosphere; | 95% |
Stage #1: 2,4-dimethylaniline-5-sulfonic acid With hydrogenchloride; sodium nitrite In water at 0℃; for 2h; Stage #2: amino-4 hydroxy-2 toluene With sodium hydroxide In water at 0℃; pH=8; | 76.9% |
Conditions | Yield |
---|---|
With 5-chloro-2-hydroxybenzoic acid; boric acid; palladium diacetate; 1,2-bis[di(t-butyl)phosphinomethyl]benzene In acetonitrile at 110℃; under 18100.7 Torr; for 48h; | 95% |
oxirane
amino-4 hydroxy-2 toluene
5-(2-hydroxyethylamino)-2-methylphenol
Conditions | Yield |
---|---|
With NaY In diethylene glycol dimethyl ether at 150℃; for 3.5h; Reagent/catalyst; Solvent; Green chemistry; | 94.1% |
2-amino-4-chloropyrimidine
amino-4 hydroxy-2 toluene
5-(2-aminopyrimidin-4-ylamino)-2-methylphenol
Conditions | Yield |
---|---|
Stage #1: 2-amino-4-chloropyrimidine; amino-4 hydroxy-2 toluene With hydrogenchloride In ethanol; water at 90℃; for 18h; Stage #2: With potassium carbonate In ethanol; water; ethyl acetate Product distribution / selectivity; | 94% |
With hydrogenchloride In ethanol; water at 80 - 90℃; Product distribution / selectivity; |
3-(1-cyanocyclopropyl)benzoyl chloride
amino-4 hydroxy-2 toluene
3-(1-cyano-1-methylethyl)-N-(3-hydroxy-4-methylphenyl)benzamide
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In tetrahydrofuran; water at 20℃; for 5h; | 94% |
5-bromo-1,3-xylene
amino-4 hydroxy-2 toluene
5-(3,5-dimethylphenylamino)-2-methylphenol
Conditions | Yield |
---|---|
With chloro[2-(dicyclohexylphosphino)-3,6-dimethoxy-2',4',6'-triisopropyl-1,1'-biphenyl][2-(2-aminoethyl)phenyl]palladium(ll); sodium t-butanolate In 1,4-dioxane at 90℃; for 1h; Inert atmosphere; | 94% |
3-(1-cyano-1-methylethyl)benzoyl chloride
amino-4 hydroxy-2 toluene
3-(1-cyano-1-methylethyl)-N-(3-hydroxy-4-methylphenyl)benzamide
Conditions | Yield |
---|---|
Stage #1: amino-4 hydroxy-2 toluene With sodium hydrogencarbonate In tetrahydrofuran; water at 20℃; Stage #2: 3-(1-cyano-1-methylethyl)benzoyl chloride In tetrahydrofuran; water at 20℃; Cooling with ice; | 94% |
1-chloro-3-methoxy-benzene
amino-4 hydroxy-2 toluene
3-[(3-methoxyphenyl)amino]-6-methylphenol
Conditions | Yield |
---|---|
With chloro[2-(dicyclohexylphosphino)-3,6-dimethoxy-2',4',6'-triisopropyl-1,1'-biphenyl][2-(2-aminoethyl)phenyl]palladium(ll); sodium t-butanolate In 1,4-dioxane at 90℃; for 1.16667h; Inert atmosphere; | 92% |
Conditions | Yield |
---|---|
With 1,3-bis-(diphenylphosphino)propane; palladium diacetate; toluene-4-sulfonic acid In tetrahydrofuran; acetonitrile at 120℃; under 23272.3 Torr; for 72h; regioselective reaction; | 92% |
4-(pyrrolidin-1-ylsulfonyl)aniline
amino-4 hydroxy-2 toluene
Conditions | Yield |
---|---|
Stage #1: 4-(pyrrolidin-1-ylsulfonyl)aniline With hydrogenchloride; isopentyl nitrite In methanol; water; acetonitrile at 0℃; for 1h; Inert atmosphere; Stage #2: amino-4 hydroxy-2 toluene With potassium carbonate In methanol; water; acetonitrile at 0℃; for 1h; | 92% |
amino-4 hydroxy-2 toluene
4-chloro-6-methoxy-quinoline-3-carbonitrile
Conditions | Yield |
---|---|
With pyridine hydrochloride In 2-ethoxy-ethanol for 1h; Heating / reflux; | 91% |
With pyridine hydrochloride In 2-ethoxy-ethanol; water | 278.3 mg (91%) |
With pyridine hydrochloride In 2-ethoxy-ethanol; water | 278.3 mg (91 %) |
3-methoxyphenyl bromide
amino-4 hydroxy-2 toluene
3-[(3-methoxyphenyl)amino]-6-methylphenol
Conditions | Yield |
---|---|
With chloro[2-(dicyclohexylphosphino)-3,6-dimethoxy-2',4',6'-triisopropyl-1,1'-biphenyl][2-(2-aminoethyl)phenyl]palladium(ll); sodium t-butanolate In 1,4-dioxane at 90℃; for 1h; Inert atmosphere; | 91% |
amino-4 hydroxy-2 toluene
benzoyl chloride
N-(3-hydroxy-4-methylphenyl)benzamide
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In water; ethyl acetate at 0℃; for 2h; Inert atmosphere; Schlenk technique; | 91% |
With triethylamine In tetrahydrofuran at 0 - 20℃; for 0.5h; | 81% |
ethyl 2-phenyldiazoacetate
amino-4 hydroxy-2 toluene
Conditions | Yield |
---|---|
With C43H37Br2CuN3P2(1+)*ClO4(1-) In methanol at 0 - 20℃; for 4h; Inert atmosphere; Schlenk technique; chemoselective reaction; | 91% |
4-Nitrophthalonitrile
amino-4 hydroxy-2 toluene
Conditions | Yield |
---|---|
With potassium carbonate In dimethyl sulfoxide at 65℃; for 6h; Inert atmosphere; | 90.8% |
amino-4 hydroxy-2 toluene
4-chloro-6-fluoro-[1,7]naphthyridine-3-carbonitrile
Conditions | Yield |
---|---|
In ethanol for 16h; | 90% |
In ethanol for 16h; | 90% |
amino-4 hydroxy-2 toluene
4-chloro-6-(4-nitrophenyl)furo[2,3-d]pyrimidine
2-methyl-5-{[6-(4-nitrophenyl)furo[2,3-d]pyrimidin-4-yl]amino}phenol
Conditions | Yield |
---|---|
In butan-1-ol for 3h; Heating; | 89% |
3,5-dimethylphenyl iodide
amino-4 hydroxy-2 toluene
3-(3,5-dimethylphenoxy)-4-methylaniline
Conditions | Yield |
---|---|
With 2-Picolinic acid; potassium phosphate; copper(l) iodide In dimethyl sulfoxide at 80℃; for 24h; Inert atmosphere; | 87% |
4-(4-aminophenyl)thiomorpholine 1,1-dioxide
amino-4 hydroxy-2 toluene
Conditions | Yield |
---|---|
Stage #1: 4-(4-aminophenyl)thiomorpholine 1,1-dioxide With hydrogenchloride; isopentyl nitrite In methanol; water; acetonitrile at 0℃; for 1h; Inert atmosphere; Stage #2: amino-4 hydroxy-2 toluene With potassium carbonate In methanol; water; acetonitrile at 0℃; for 1h; | 87% |
2-chloropyrimidin-4-amine
amino-4 hydroxy-2 toluene
5-(4-aminopyrimidin-2-ylamino)-2-methylphenol
Conditions | Yield |
---|---|
Stage #1: 2-chloropyrimidin-4-amine; amino-4 hydroxy-2 toluene With hydrogenchloride In ethanol; water at 90℃; for 18h; Stage #2: With potassium carbonate In ethanol; water; ethyl acetate Product distribution / selectivity; | 86% |
With hydrogenchloride In ethanol; water at 80 - 90℃; Product distribution / selectivity; |
1-Chloro-4-fluorobenzene
amino-4 hydroxy-2 toluene
3-[(4-fluorophenyl)amino]-6-methylphenol
Conditions | Yield |
---|---|
With chloro[2-(dicyclohexylphosphino)-3,6-dimethoxy-2',4',6'-triisopropyl-1,1'-biphenyl][2-(2-aminoethyl)phenyl]palladium(ll); sodium t-butanolate In 1,4-dioxane at 90℃; for 1.16667h; Inert atmosphere; | 86% |
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