Unique advantages for 4'-Aminoacetanilide Cas 122-80-5 Guaranteed the purity High quality & competitive price Quality control Fast feedback Prompt shipment Appearance:Powder Package:1kg/foil bag, 25kg/drum or as you required
Cas:122-80-5
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inquiryimg heightAppearance:detailed see specifications Storage:Store in dry, dark and ventilated place. Package:according to the clients requirement Application:Used in Synthesis, Pharmaceuticals and other fields Transportation:by air or by sea Port:Shan
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Cas:122-80-5
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Cas:122-80-5
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inquiry2-Deoxy-L-ribose Basic information Product Name: 2-Deoxy-L-ribose Synonyms: 2-DEOXY-L-RIBOSE;L-ERYTHRO-PENTOFURANOSE;2-DEOXY-L-RIBOSE 99%;L-erythro-Pentose, 2-deoxy-;2-Deoxy-L-ribose,99%
Cas:122-80-5
Min.Order:100 Kilogram
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inquiryProduct Name: 4'-Aminoacetanilide Synonyms: 1-Amino-4-(acetylamino)benzene;4’-aminoacetanilid;4’-amino-acetanilid;4-Acetoamidoaniline;4'-Aminoacetanilid;Acetamide,N-(4-aminophenyl)-;Acet
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
Cas:122-80-5
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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
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:122-80-5
Min.Order:10 Gram
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inquirySuperior quality, moderate price & quick delivery. Appearance:pink to brown fine crystalline powder Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:1kg/bag, 1kg/drum or 25kg/drum or as per your request. Applic
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Min.Order:1 Kilogram
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Min.Order:1 Gram
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high quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
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:122-80-5
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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inquiryAmoychem is committed to providing the top-quality chemical products and services Internationally. We offer our customers with friendly, professional service and reliable, high performance products that have been manufactured according to the accredi
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Cas:122-80-5
Min.Order:10 Milligram
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inquiryCAS: 122-80-5 MF: C8H10N2O MW: 150.18 EINECS: 204-576-6 Properties Melting point: 164-167 °C(lit.) Boiling point: 267 °C Density
Cas:122-80-5
Min.Order:1 Metric Ton
Negotiable
Type:Trading Company
inquiry4'-Aminoacetanilide Basic information Product Name: 4'-Aminoacetanilide Synonyms: 1-Amino-4-(acetylamino)benzene;4’-aminoacetanilid;4’-amino-acetanilid;4-Acetoamidoaniline;4'-Amino
Changzhou Extraordinary Pharmatech co., LTD. As a leading chemical manufacturer and supplier in China.DAS authentication is passed.We can provide the popular precursor chemicals, we have our own strong R & D team, have our own laboratories and fa
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Conditions | Yield |
---|---|
With hydrazine hydrate; nickel In methanol for 6h; | 100% |
With indium; acetic acid In tetrahydrofuran Heating; | 100% |
With trimethylamine-borane; palladium hydroxide - carbon In methanol for 3.5h; Heating; | 99% |
acetic acid
ethyl acetate
1,4-phenylenediamine
N-acetyl-p-phenylenediamine
Conditions | Yield |
---|---|
With 1,4-diaza-bicyclo[2.2.2]octane at 65 - 90℃; for 6h; Time; Inert atmosphere; | 98.6% |
p-aminoacetophenone oxime
N-acetyl-p-phenylenediamine
Conditions | Yield |
---|---|
With chlorosulfonic acid In toluene at 90℃; for 0.5h; Beckmann rearrangement; | 98% |
With trifluoromethylsulfonic anhydride In dichloromethane at 20℃; for 3h; Beckmann Rearrangement; Inert atmosphere; | 94% |
With iodine In acetonitrile for 4h; Beckmann rearrangement; Reflux; | 90% |
Conditions | Yield |
---|---|
at 20℃; | 95% |
In dichloromethane at 20℃; Inert atmosphere; | 95% |
In tetrahydrofuran at 20℃; | 65% |
Conditions | Yield |
---|---|
With bis(triphenylphosphine)nickel(II) chloride; lithium hexamethyldisilazane In 1,4-dioxane at 90℃; for 2h; Glovebox; Sealed tube; | 91% |
Stage #1: 4-bromoacetanilide With lithium hexamethyldisilazane; DavePhos; tris(dibenzylideneacetone)dipalladium (0) In 1,4-dioxane at 100℃; for 17h; Stage #2: With hydrogenchloride In 1,4-dioxane at 20℃; for 0.0833333h; Further stages.; | 70% |
Conditions | Yield |
---|---|
With ammonium hydroxide; potassium phosphate; 1-(5,6,7,8-tetrahydroquinolin-8-yl)-2-methylpropan-1-one; copper(I) bromide In dimethyl sulfoxide at 25℃; for 24h; Inert atmosphere; Sealed tube; | 90% |
Conditions | Yield |
---|---|
With ammonium hydroxide; potassium phosphate In dimethyl sulfoxide at 80℃; UV-irradiation; | 89% |
1,4-phenylenediamine
A
4-nitro-N-(4-chlorophenyl)benzenesulfonamide
B
N-acetyl-p-phenylenediamine
Conditions | Yield |
---|---|
With potassium carbonate In water at 80℃; for 2h; Green chemistry; chemoselective reaction; | A n/a B 86% |
N-(4-azido-phenyl)acetamide
N-acetyl-p-phenylenediamine
Conditions | Yield |
---|---|
With iron(III) oxide; hydrazine hydrate In water at 120℃; for 1.5h; Inert atmosphere; | 85% |
2-[(4-acetylaminophenylamino)methylene]malonic acid diethyl ester
N-acetyl-p-phenylenediamine
Conditions | Yield |
---|---|
With ethylenediamine In ethanol at 20℃; for 1.3h; | 80% |
N-(4-oxocyclohexyl)acetamide
N-acetyl-p-phenylenediamine
Conditions | Yield |
---|---|
With ethene; 5%-palladium/activated carbon; ammonium acetate; potassium carbonate In acetonitrile at 90℃; under 760.051 Torr; for 15h; Reagent/catalyst; Schlenk technique; | 80% |
With styrene; ammonium hydroxide In 1-methyl-pyrrolidin-2-one at 130℃; for 20h; Sealed tube; Inert atmosphere; | 65% |
Conditions | Yield |
---|---|
A n/a B 76% |
4-(+/-)-α-hydroxyethylphenylacetamide
N-acetyl-p-phenylenediamine
Conditions | Yield |
---|---|
With sodium azide; trifluoroacetic acid In hexane at 40℃; for 4h; Sealed tube; | 76% |
With sodium azide; methanesulfonic acid; trifluoroacetic acid In hexane at 40℃; for 12h; | 76% |
Conditions | Yield |
---|---|
With 10-methyl-9-(2,4,6-trimethylphenyl) acridinium tetrafluoroborate In acetonitrile at 20℃; for 5h; Irradiation; | 75% |
With 10-methyl-9-(2,4,6-trimethylphenyl) acridinium tetrafluoroborate In acetonitrile at 20℃; for 5h; Irradiation; | 75% |
acetic anhydride
1,4-phenylenediamine
A
N,N'-diacetyl-1,4-phenylenediamine
B
N-acetyl-p-phenylenediamine
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 24h; | A 7% B 63% |
Conditions | Yield |
---|---|
With hydroxylamine triflate; iron(II) sulfate In water; acetonitrile at 20℃; for 16h; | 62% |
Conditions | Yield |
---|---|
With copper(l) iodide; water; caesium carbonate; potassium hydroxide; N,N`-dimethylethylenediamine at 100℃; for 15h; Inert atmosphere; Schlenk technique; | 58% |
Conditions | Yield |
---|---|
With nitromethane; trifluoromethylsulfonic anhydride; acetic acid In formic acid at 80 - 120℃; | 50% |
1-(4-aminophenyl)ethanone oxime
N-acetyl-p-phenylenediamine
Conditions | Yield |
---|---|
With 1,1,1,3',3',3'-hexafluoro-propanol; tetrabutylammonium tetrafluoroborate; water In 1,2-dichloro-ethane at 20℃; for 0.733333h; Beckmann Rearrangement; Electrochemical reaction; | 31% |
N-(4-Butylamino-phenyl)-acetamide
A
butyraldehyde
B
N-acetyl-p-phenylenediamine
Conditions | Yield |
---|---|
With oxygen; salcomine In methanol for 24h; Heating; | A n/a B 24% |
N-(4-Nitrophenyl)acetamide
A
N-acetyl-p-phenylenediamine
B
bis-(4-acetylamino-phenyl)-diazene-N-oxide
Conditions | Yield |
---|---|
durch elektrolytische Reduktion; |
sodium acetate
p-phenylenediamine hydrochloride
N-acetyl-p-phenylenediamine
Conditions | Yield |
---|---|
With water |
p-toluenesulfonyl chloride
N-acetyl-p-phenylenediamine
N-(4-(4-methylphenylsulfonamido)phenyl)acetamide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 4℃; | 100% |
With pyridine In N,N-dimethyl-formamide; benzene for 24h; Ambient temperature; | |
With pyridine In dichloromethane at 20℃; |
carbon disulfide
N-acetyl-p-phenylenediamine
4-(N-acetylamino)phenyl isothiocyanate
Conditions | Yield |
---|---|
Stage #1: carbon disulfide; N-acetyl-p-phenylenediamine With triethylamine In ethanol at 20℃; Stage #2: With dmap; di-tert-butyl dicarbonate In ethanol at 20℃; for 0.25h; Further stages.; | 100% |
Stage #1: carbon disulfide; N-acetyl-p-phenylenediamine With triethylamine In ethanol at 20℃; for 1h; Stage #2: With dmap; di-tert-butyl dicarbonate at 0℃; for 2h; | |
Stage #1: carbon disulfide; N-acetyl-p-phenylenediamine With triethylamine In tetrahydrofuran at 20℃; Stage #2: With dmap; di-tert-butyl dicarbonate In tetrahydrofuran at 0 - 20℃; | 100 %Chromat. |
Stage #1: carbon disulfide; N-acetyl-p-phenylenediamine With triethylamine In ethanol at 20℃; for 2h; Stage #2: With dmap; di-tert-butyl dicarbonate In ethanol at 20℃; for 2h; |
Conditions | Yield |
---|---|
With ammonium bromide; ethylenediamine at 70℃; for 5h; Microwave irradiation; Inert atmosphere; neat (no solvent); | 99% |
With ammonium iodide; hydrazine at 50℃; for 12h; | 99% |
With ammonium iodide; hydrazine hydrate at 50℃; for 12h; Inert atmosphere; Sealed tube; | 99% |
N-acetyl-p-phenylenediamine
hexadecanyl bromide
N-(4-dihexadecylaminophenyl)acetamide
Conditions | Yield |
---|---|
With sodium carbonate In 2-methoxy-ethanol | 99% |
With sodium hydrogencarbonate In N,N-dimethyl-formamide at 120℃; for 14h; | 82% |
(hex-1-en-3-yl)methyl carbonate
N-acetyl-p-phenylenediamine
Conditions | Yield |
---|---|
With cobalt(II) tetrafluoroborate; C36H29N2O2P; zinc In acetonitrile at 20℃; for 16h; Inert atmosphere; Sealed tube; enantioselective reaction; | 99% |
5-nitro-2-furoyl isothiocyanate
N-acetyl-p-phenylenediamine
N-{4-[3-(5-Nitro-furan-2-carbonyl)-thioureido]-phenyl}-acetamide
Conditions | Yield |
---|---|
In diethyl ether for 27h; Ambient temperature; | 98% |
Conditions | Yield |
---|---|
Stage #1: piperonal; N-acetyl-p-phenylenediamine With Decaborane In methanol at 20℃; for 0.5h; Stage #2: formaldehyd With Decaborane In methanol; water at 20℃; for 1.5h; | 98% |
N-acetyl-p-phenylenediamine
Conditions | Yield |
---|---|
Stage #1: 4-(4-(4-(4-(((6aS)-5-((allyloxy)carbonyl)-2-methoxy-12-oxo-6-((tetrahydro-2H-pyran-2-yl)oxy)-5,6,6a,7,8,9,10,12-octahydrobenzo[e]pyrido[1,2-a][1,4] diazepin-3-yl)oxy)butanamido)-1-methyl-1H-pyrrole-2- carboxamido)phenyl)-1-methyl-1H-pyrrole-2-carboxylic acid With triethylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In dichloromethane at 20℃; for 0.25h; Stage #2: N-acetyl-p-phenylenediamine In dichloromethane at 20℃; for 1.5h; | 98% |
leucoquinizarin
1,4-dihydroxy-9,10-anthracenedione
N-acetyl-p-phenylenediamine
Conditions | Yield |
---|---|
Stage #1: N-acetyl-p-phenylenediamine With hydrogenchloride In water at 40 - 50℃; for 0.5h; Stage #2: leucoquinizarin; 1,4-dihydroxy-9,10-anthracenedione In water at 85 - 90℃; Solvent; Temperature; | 97.13% |
5-nitro-3-furanoyl chloride
N-acetyl-p-phenylenediamine
5-Nitro-furan-3-carboxylic acid (4-acetylamino-phenyl)-amide
Conditions | Yield |
---|---|
In 1,4-dioxane at 10 - 15℃; for 3h; | 97% |
p-tolyllead triacetate
N-acetyl-p-phenylenediamine
N-{4-[(4-methylphenyl)amino]phenyl}acetamide
Conditions | Yield |
---|---|
copper diacetate In dichloromethane at 25℃; for 1h; Arylation; | 97% |
anthranilic acid
orthoformic acid triethyl ester
N-acetyl-p-phenylenediamine
N-{4-[4-oxo-3(4H)-quinazolinyl]phenyl}acetamide
Conditions | Yield |
---|---|
With ytterbium(III) triflate at 60℃; for 0.0333333h; | 97% |
acetonitrile
N-acetyl-p-phenylenediamine
A
N-(4-diethylamino-phenyl)-acetamide
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In methanol at 20℃; for 12h; | A n/a B 97% |
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; hydrogen In ethyl acetate at 20℃; under 760.051 Torr; for 12h; | 97% |
methanol
N-acetyl-p-phenylenediamine
N'-acetyl-N,N-dimethyl-1,4-phenylenediamine
Conditions | Yield |
---|---|
With C15H29IrN4(2+)*2I(1-) at 120℃; for 17h; Inert atmosphere; Schlenk technique; Sealed tube; | 97% |
3-formyl-6-methylchromone
N-acetyl-p-phenylenediamine
Conditions | Yield |
---|---|
With acetic acid In ethanol for 7h; Reflux; | 97% |
5-nitro-3-furoyl isothiocyanate
N-acetyl-p-phenylenediamine
N-{4-[3-(5-Nitro-furan-3-carbonyl)-thioureido]-phenyl}-acetamide
Conditions | Yield |
---|---|
In diethyl ether for 27h; Ambient temperature; | 96% |
5-(2-chlorophenyl)-2-furoyl chloride
N-acetyl-p-phenylenediamine
Conditions | Yield |
---|---|
With PEG-400; sodium hydroxide In dichloromethane at 20℃; for 1h; Acylation; | 96% |
4-chloro-6-nitroquinoline
N-acetyl-p-phenylenediamine
4-[4-(acetylamino)anilino]-6-nitroquinolinium chloride
Conditions | Yield |
---|---|
With hydrogenchloride In 1,4-dioxane; ethanol for 0.5h; Heating / reflux; | 96% |
diethyl 2-ethoxymethylenemalonate
N-acetyl-p-phenylenediamine
2-[(4-acetylaminophenylamino)methylene]malonic acid diethyl ester
Conditions | Yield |
---|---|
for 1h; Heating; | 95% |
1-(4-nitrophenyl)pyrrole-2-carbaldehyde
N-acetyl-p-phenylenediamine
N-(4-{[1-[1-(4-Nitro-phenyl)-1H-pyrrol-2-yl]-meth-(E)-ylidene]-amino}-phenyl)-acetamide
Conditions | Yield |
---|---|
With sodium sulfate In benzene for 20h; Heating; | 95% |
pyruvic acid methyl ester
N-acetyl-p-phenylenediamine
1-(4-Acetylamino-phenyl)-4-(4-acetylamino-phenylamino)-2-methyl-5-oxo-2,5-dihydro-1H-pyrrole-2-carboxylic acid methyl ester
Conditions | Yield |
---|---|
In dichloromethane at 20 - 25℃; for 1h; Irradiation; | 95% |
N-acetyl-p-phenylenediamine
tert-butylcarbamoyl-thioacetic acid S-tert-butyl ester
Conditions | Yield |
---|---|
With silver trifluoroacetate In 1,2-dimethoxyethane at 20℃; | 95% |
di-tert-butyl dicarbonate
N-acetyl-p-phenylenediamine
(4-acetylaminophenyl)carbamic acid tert-butyl ester
Conditions | Yield |
---|---|
With zinc(II) perchlorate In tert-butyl alcohol at 20℃; for 72h; | 95% |
With PEG-400 at 20℃; for 2h; Neat (no solvent); chemoselective reaction; | 86% |
With 1-butyl-3-methylimidazolium trifluoromethanesulfonimide at 30 - 35℃; for 0.75h; neat (no solvent); chemoselective reaction; | 80% |
2,6-Dichloropyrimidine
N-acetyl-p-phenylenediamine
N-(4-(2-chloropyrimidin-4-ylamino)phenyl)acetamide
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In tetrahydrofuran; ethanol at 75℃; | 95% |
With sodium hydrogencarbonate In tetrahydrofuran; ethanol at 0 - 20℃; for 16h; |
2,5-dinitropyridine
N-acetyl-p-phenylenediamine
N-[4-(5-nitropyridin-2-ylamino)phenyl]acetamide
Conditions | Yield |
---|---|
In ethanol; acetic acid at 20℃; for 2h; | 95% |
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