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3-(butylamino)-4-chloro-5-sulfamoylbenzoic acid

Base Information
  • Chemical Name:3-(butylamino)-4-chloro-5-sulfamoylbenzoic acid
  • CAS No.:22893-29-4
  • Molecular Formula:C11H15 Cl N2 O4 S
  • Molecular Weight:306.77
  • Hs Code.:
  • Mol file:22893-29-4.mol
3-(butylamino)-4-chloro-5-sulfamoylbenzoic acid

Synonyms:Benzoicacid, 3-(butylamino)-4-chloro-5-sulfamoyl- (8CI);3-(Butylamino)-4-chloro-5-sulfamoylbenzoic acid;3-n-Butylamino-4-chloro-5-sulfamoylbenzoic acid; HH 594

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Chemical Property of 3-(butylamino)-4-chloro-5-sulfamoylbenzoic acid
Chemical Property:
  • Vapor Pressure:1.31E-13mmHg at 25°C 
  • Boiling Point:565.1°Cat760mmHg 
  • Flash Point:295.6°C 
  • Density:1.448g/cm3 
Purity/Quality:
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MSDS Files:

SDS file from LookChem

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Technology Process of 3-(butylamino)-4-chloro-5-sulfamoylbenzoic acid

There total 6 articles about 3-(butylamino)-4-chloro-5-sulfamoylbenzoic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
3-butylamino-4-chloro-5-(dimethylaminomethylene-sulfamoyl)-benzoic acid methyl ester; With water; sodium hydroxide; In methanol; at 50 ℃; for 2h;
With hydrogenchloride; In water;
Guidance literature:
Multi-step reaction with 6 steps
1: thionyl chloride / 50 °C
2: acetonitrile / 20 °C
3: water; ammonium chloride; iron / ethanol / 2.05 h / 85 °C
4: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 2 h / 20 °C
5: borane-THF / tetrahydrofuran / 1 h / 20 °C
6: sodium hydroxide; water / methanol / 2 h / 50 °C
With thionyl chloride; borane-THF; water; iron; ammonium chloride; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In tetrahydrofuran; methanol; ethanol; acetonitrile;
Guidance literature:
Multi-step reaction with 5 steps
1: acetonitrile / 20 °C
2: water; ammonium chloride; iron / ethanol / 2.05 h / 85 °C
3: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 2 h / 20 °C
4: borane-THF / tetrahydrofuran / 1 h / 20 °C
5: sodium hydroxide; water / methanol / 2 h / 50 °C
With borane-THF; water; iron; ammonium chloride; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In tetrahydrofuran; methanol; ethanol; acetonitrile;
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