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3-Methyl-4-aminobenzensulfonamide

3-Methyl-4-aminobenzensulfonamide Suppliers list
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Products Intro: Product Name:3-Methyl-4-aminobenzensulfonamide
CAS:53297-70-4
Purity:98% Package:1KG;1USD
Company Name: Jinan Carbotang Biotech Co.,Ltd.
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Products Intro: Product Name:4-amino-3-methylbenzenesulfonamide
CAS:53297-70-4
Purity:98% Package:5KG;1KG
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Products Intro: Product Name:3-Methyl-4-aminobenzensulfonamide
CAS:53297-70-4
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Products Intro: Product Name:4-Amino-3-methylbenzenesulfonamide
CAS:53297-70-4
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-00257
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Products Intro: Product Name:3-Methyl-4-aminobenzensulfonamide
CAS:53297-70-4
Purity:99.0% Package:100g;1kg;5kg;25kg

3-Methyl-4-aminobenzensulfonamide manufacturers

3-Methyl-4-aminobenzensulfonamide Basic information
Product Name:3-Methyl-4-aminobenzensulfonamide
Synonyms:3-METHYL-4-AMINOBENZENSULFONAMIDE;4-AMINO-3-METHYLBENZENESULPHONAMIDE;4-AMINO-3-METHYLBENZENSULFONAMIDE;3-Methyl-4-aminobenzensulfonamide 4-amino-3-methylbenzenesulfonamide;3-METHYL-4-AMINOBENZENSULFONAMIDE 98+%;BenzenesulfonaMide, 4-aMino-3-Methyl-;4-aMino-3-Methylbenzene-1-sulfonaMide;4-(Aminosulphonyl)-2-methylaniline, 2-Amino-5-(aminosulphonyl)toluene
CAS:53297-70-4
MF:C7H10N2O2S
MW:186.23
EINECS:
Product Categories:Phenyls & Phenyl-Het;Miscellaneous;Phenyls & Phenyl-Het;SULFONAMIDE
Mol File:53297-70-4.mol
3-Methyl-4-aminobenzensulfonamide Structure
3-Methyl-4-aminobenzensulfonamide Chemical Properties
Melting point 174 °C
Boiling point 409.3±55.0 °C(Predicted)
density 1.359±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
pka10.19±0.60(Predicted)
CAS DataBase Reference53297-70-4(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Hazard Note Irritant
HS Code 2935909099
MSDS Information
3-Methyl-4-aminobenzensulfonamide Usage And Synthesis
Synthesis
4-Amino-3-methyl-benzenesulfonamide

252562-03-1

3-Methyl-4-aminobenzensulfonamide

53297-70-4

N-(2-methyl-4-aminosulfonylphenyl)acetamide (5.1 g, 22.3 mmol) was used as a raw material, which was mixed with 2N hydrochloric acid (76.5 ml) and ethanol (100 ml) and the reaction was carried out at reflux overnight. Upon completion of the reaction, the reaction mixture was neutralized with aqueous sodium carbonate to pH=8. Subsequently, the mixture was extracted with ethyl acetate (80 mL x 4), the organic phases were combined and dried over anhydrous sodium sulfate. The organic phase was concentrated under reduced pressure to afford 4-amino-3-methylbenzenesulfonamide as a light-colored solid (4.9 g, 100% yield).

References[1] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 6, p. 2338 - 2342
[2] Patent: US9138427, 2015, B2. Location in patent: Page/Page column 304
[3] Patent: EP1208091, 2006, B1. Location in patent: Page/Page column 8; 21
[4] Collection of Czechoslovak Chemical Communications, 1948, vol. 13, p. 161,165,169
[5] Journal of Medicinal Chemistry, 2004, vol. 47, # 5, p. 1175 - 1182
3-Methyl-4-aminobenzensulfonamide Preparation Products And Raw materials
Raw materials4-Amino-3-methyl-benzenesulfonamide-->Hydrochloric acid-->Water-->Ethanol
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