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Cas:950-58-3
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inquiry4-amino-2,6-di-tert-butylphenol CAS:950-58-3 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 org
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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
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inquiryhigh 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
Hangzhou Dingyan Chem is a leading manufacturer and supplier of chemicals in China.We develop,produce and distribute high quality pharmaceuticals, intermediates, special chemicals and other fine chemicals. We could give you: 1.Best quality in your re
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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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inquiryWe product this chemical more than 10 years . We are very experience to export it to many countries, Our superior & stable quality , competitive price gain warm reception from our customers. Application:Pharm intermediate
4-Amino-2,6-ditert-butyl-phenol cas 950-58-3Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
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Our mission is to provide high-quality and innovative products to our customers. By offering a broad range of products, custom synthesis and personalized services, Bide can help scientists speeding up their research in the chemical and pharmaceutical
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inquiryApplication: It is an important raw material and in... DeliveryTime: prompt PackAge: according to the clients requirement Port: Shanghai ProductionCapacity: 1-10 Metric Ton/Month Purity: 99.8% Storage: Sto
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2,6-di-tert-butyl-1,4-benzoquinone monooxime
2,6-di-tert-butyl-4-aminophenol
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; hydrogen In ethanol at 20℃; under 760.051 Torr; | 80% |
With hydrogen; platinum In 1,4-dioxane | |
Multi-step reaction with 2 steps 1: 2 h / 180 - 185 °C 2: acid hydrolysis View Scheme | |
With palladium 10% on activated carbon; hydrogen; trifluoroacetic acid In methanol under 760.051 Torr; for 2h; Inert atmosphere; |
Conditions | Yield |
---|---|
With hydrogen; palladium on activated carbon In ethanol; dichloromethane at 30℃; under 1034.32 Torr; for 2h; | 50% |
With hydrogen; palladium 10% on activated carbon In ethanol; dichloromethane at 20℃; under 1034.32 Torr; for 2h; | 50% |
With hydrogen; palladium 10% on activated carbon In ethanol; dichloromethane at 20℃; under 1034.32 Torr; for 2h; | 50% |
Conditions | Yield |
---|---|
With hydrogen; nickel | |
With sodium hydroxide; sodium dithionite at 45 - 60℃; | |
With potassium hydroxide; sodium hydrogensulfide | |
With sodium dithionite; sodium hydroxide In water at 30 - 65℃; for 1h; Reagent/catalyst; Temperature; Inert atmosphere; |
3,5-di-tert-butyl-4-hydroxyformanilide
2,6-di-tert-butyl-4-aminophenol
Conditions | Yield |
---|---|
acid hydrolysis; Yield given; |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 95 percent / 2 h / 180 - 185 °C 2: acid hydrolysis View Scheme | |
Multi-step reaction with 2 steps 1: hydroxylamine 2: 5percent sodium hydroxide, sodium dithionite / 45 - 60 °C View Scheme |
2,6-di-tert-butyl-4-(phenylimino)cyclohexa-2,5-dienone
2,6-di-tert-butyl-4-aminophenol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 2 h / 180 - 185 °C 2: acid hydrolysis View Scheme |
2,6-di-tert-butyl-4-(3,5-di-tert-butyl-4-hydroxyphenylimino)-2,5-cyclohexadien-1-one
2,6-di-tert-butyl-4-aminophenol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 2 h / 180 - 185 °C 2: acid hydrolysis View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 16.2 percent / chromic anhydride 2: hydroxylamine 3: 5percent sodium hydroxide, sodium dithionite / 45 - 60 °C View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 2: H2 / Raney-Ni View Scheme | |
Multi-step reaction with 2 steps 1: N2O4 / benzene; petroleum ether 2: Zn, aq. HCl View Scheme | |
Stage #1: 2,6-di-tert-butylphenol With hydrogenchloride; sodium hydroxide; sodium carbonate; sodium nitrite; 4-aminobenzene sulfonic acid In water at 0℃; for 1h; Stage #2: With sodium dithionite In water at 80℃; |
2,6-di-tert-butyl-4-aminophenol
4-methoxy-benzoyl chloride
N-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-4-methoxy-benzamide
Conditions | Yield |
---|---|
With triethylamine In benzene at 35 - 40℃; for 1h; | 96% |
2,6-di-tert-butyl-4-aminophenol
4-nitro-benzoyl chloride
2,6-di-tert-butyl-4-(4-nitrobenzoylamino)phenol
Conditions | Yield |
---|---|
With triethylamine In benzene at 35 - 40℃; for 1h; | 94% |
With triethylamine In diethyl ether |
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine In dichloromethane for 6h; | 92% |
2,6-di-tert-butyl-4-aminophenol
4-methyl-benzoyl chloride
N-(3,5-di-tert-butyl-4-hydroxyphenyl)-4-methylbenzamide
Conditions | Yield |
---|---|
With triethylamine In benzene at 35 - 40℃; for 1h; | 90% |
2,6-di-tert-butyl-4-aminophenol
benzoyl chloride
4-(N-benzoylamino)-2,6-di-t-butylphenol
Conditions | Yield |
---|---|
With triethylamine In benzene at 35 - 40℃; for 1h; | 87% |
2,6-di-tert-butyl-4-aminophenol
4-chloro-benzoyl chloride
N-(3,5-di-tert-butyl-4-hydroxyphenyl)-4-chlorobenzamide
Conditions | Yield |
---|---|
With triethylamine In benzene at 35 - 40℃; for 1h; | 86% |
bis(trichloromethyl) carbonate
2,6-di-tert-butyl-4-aminophenol
N-amino-(4-nitrophenyl)carboxamide
Conditions | Yield |
---|---|
With sodium chloride; N-ethyl-N,N-diisopropylamine In n-heptane; dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide | 86% |
Stage #1: bis(trichloromethyl) carbonate; 2,6-di-tert-butyl-4-aminophenol With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 0.0833333h; Stage #2: N-amino-(4-nitrophenyl)carboxamide With N-ethyl-N,N-diisopropylamine In DMF (N,N-dimethyl-formamide) at 20℃; for 4h; | 86% |
bis(trichloromethyl) carbonate
2,6-di-tert-butyl-4-aminophenol
N-amino-(4-nitrophenyl)carboxamide
Conditions | Yield |
---|---|
Stage #1: bis(trichloromethyl) carbonate; 2,6-di-tert-butyl-4-aminophenol With N-ethyl-N,N-diisopropylamine In dichloromethane Stage #2: N-amino-(4-nitrophenyl)carboxamide With N-ethyl-N,N-diisopropylamine In DMF (N,N-dimethyl-formamide); dichloromethane at 20℃; for 4h; | 86% |
Conditions | Yield |
---|---|
In DMF (N,N-dimethyl-formamide) at 23℃; for 2h; | 83% |
Conditions | Yield |
---|---|
With triethylamine In various solvent(s) at 40 - 45℃; for 2h; | 81% |
bis(trichloromethyl) carbonate
2-(p-nitrophenyl)ethylamine
2,6-di-tert-butyl-4-aminophenol
Conditions | Yield |
---|---|
Stage #1: bis(trichloromethyl) carbonate; 2,6-di-tert-butyl-4-aminophenol Stage #2: 2-(p-nitrophenyl)ethylamine | 80% |
Stage #1: bis(trichloromethyl) carbonate; 2,6-di-tert-butyl-4-aminophenol With N-ethyl-N,N-diisopropylamine Stage #2: 2-(p-nitrophenyl)ethylamine With N-ethyl-N,N-diisopropylamine | 80% |
2,6-di-tert-butyl-4-aminophenol
(4,6-Dichloro-[1,3,5]triazin-2-yl)-(4-dodecyl-phenyl)-amine
C49H74N6O2
Conditions | Yield |
---|---|
With sodium hydroxide In acetone for 6h; Heating; | 74% |
2,6-di-tert-butyl-4-aminophenol
4-nitrobenzyl isocyanate
N-[3,5-bis-(1,1-dimethylethyl)-4-hydroxyphenyl]-N'-[(4-nitrophenyl)methyl]-urea
Conditions | Yield |
---|---|
In chloroform at 20℃; for 2h; | 72% |
In chloroform at 20℃; for 2h; |
2,6-di-tert-butyl-4-aminophenol
N-[3,5-bis-(1,1-dimethylethyl)-4-hydroxyphenyl]-N'-[(4-nitrophenyl)methyl]-urea
Conditions | Yield |
---|---|
In chloroform | 72% |
2,6-di-tert-butyl-4-aminophenol
6-chloro-N2,N4-diisobutyl-1,3,5-triazine-2,4-diamine
4-(4,6-Bis-isobutylamino-[1,3,5]triazin-2-ylamino)-2,6-di-tert-butyl-phenol
Conditions | Yield |
---|---|
With sodium hydroxide In acetone Heating; | 67% |
2,6-di-tert-butyl-4-aminophenol
6-(4-hydroxy-3,5-di-tert-butylphenylamino)-2,4-dichloro-1,3,5-triazine
2,4,6-tris-(4-hydroxy-3,5-di-tert-butylanilino)-sym-triazine
Conditions | Yield |
---|---|
With sodium hydroxide In acetone for 6h; Heating; | 67% |
Conditions | Yield |
---|---|
Condensation; | 67% |
2,6-di-tert-butyl-4-aminophenol
2,4-di-(N-methyloctadecylamino)-6-chloro-sym-triazine
4-[4,6-Bis-(methyl-octadecyl-amino)-[1,3,5]triazin-2-ylamino]-2,6-di-tert-butyl-phenol
Conditions | Yield |
---|---|
With sodium hydroxide In acetone Heating; | 66% |
With potassium hydroxide 1.) dioxane, reflux, 3 h, 2.) dioxane, reflux, 1 h; Yield given; Multistep reaction; |
3-{4-[(1,1-dimethylethoxy)carbonyl]aminophenoxy}azetidine
2,6-di-tert-butyl-4-aminophenol
Conditions | Yield |
---|---|
Stage #1: 2,6-di-tert-butyl-4-aminophenol With bis(trichloromethyl) carbonate In dichloromethane at 23℃; for 1.08333h; Stage #2: 3-{4-[(1,1-dimethylethoxy)carbonyl]aminophenoxy}azetidine With N-ethyl-N,N-diisopropylamine In dichloromethane at 23℃; for 2h; | 61% |
2,6-di-tert-butyl-4-aminophenol
(+)-usnic acid
Conditions | Yield |
---|---|
In ethanol at 80℃; for 4h; Inert atmosphere; | 61% |
2,6-di-tert-butyl-4-aminophenol
2-(N-methyloctadecylamino)-4,6-dichloro-sym-triazine
C50H84N6O2
Conditions | Yield |
---|---|
With sodium hydroxide In acetone for 6h; Heating; | 59% |
With potassium hydroxide 1.) dioxane, reflux, 3 h, 2.) dioxane, reflux, 1 h; Yield given; Multistep reaction; |
benzenesulphinyl chloride
2,6-di-tert-butyl-4-aminophenol
N-(phenylsulfinyl)-2,6-di-tert-butyl-1,4-benzoquinone imine
Conditions | Yield |
---|---|
Stage #1: benzenesulphinyl chloride; 2,6-di-tert-butyl-4-aminophenol With triethylamine In diethyl ether for 0.166667h; Stage #2: With silver(l) oxide In acetone for 0.5h; Further stages.; | 58% |
4-methylbenzenesulfinyl chloride
2,6-di-tert-butyl-4-aminophenol
N-[(4-methylphenyl)sulfinyl]-2,6-di-tert-butyl-1,4-benzoquinone imine
Conditions | Yield |
---|---|
Stage #1: 4-methylbenzenesulfinyl chloride; 2,6-di-tert-butyl-4-aminophenol With triethylamine In diethyl ether for 0.166667h; Stage #2: With silver(l) oxide In acetone for 0.5h; Further stages.; | 58% |
2,6-di-tert-butyl-4-aminophenol
3,4,5-Trimethoxybenzoyl chloride
N-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-3,4,5-trimethoxy-benzamide
Conditions | Yield |
---|---|
With triethylamine In benzene at 35 - 40℃; for 1h; | 57% |
2,6-di-tert-butyl-4-aminophenol
5-(4-nitrophenyl)-furan-2-carboxylic acid
Conditions | Yield |
---|---|
Stage #1: 5-(4-nitrophenyl)-furan-2-carboxylic acid Stage #2: 2,6-di-tert-butyl-4-aminophenol | 56% |
1,3,5-trichloro-2,4,6-triazine
2,6-di-tert-butyl-4-aminophenol
6-(4-hydroxy-3,5-di-tert-butylphenylamino)-2,4-dichloro-1,3,5-triazine
Conditions | Yield |
---|---|
With sodium hydroxide In water; acetone 1. 0 deg C, 1 h; 2. 20 deg C, 1 h; | 54% |
With sodium carbonate at 0 - 5℃; for 0.166667h; Inert atmosphere; |
p-chlorophenylsulfinyl chloride
2,6-di-tert-butyl-4-aminophenol
N-[(4-chlorophenyl)sulfinyl]-2,6-di-tert-butyl-1,4-benzoquinone imine
Conditions | Yield |
---|---|
Stage #1: p-chlorophenylsulfinyl chloride; 2,6-di-tert-butyl-4-aminophenol With triethylamine In diethyl ether for 0.166667h; Stage #2: With silver(l) oxide In acetone for 0.5h; Further stages.; | 54% |
2,6-di-tert-butyl-4-aminophenol
2-azido-5-nitrobenzaldehyde
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide for 0.333333h; Heating; | 53% |
Conditions | Yield |
---|---|
In ethanol Heating; | 52% |
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