42760-43-0

Basic information

• Product Name: 4-amino-3,5-dinitrobenzenesulfonyl chloride
• Synonyms: 4-amino-3,5-dinitrobenzenesulfonyl chloride
• CAS NO: 42760-43-0
• Molecular Weight: 281.633
• Mol File: 42760-43-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 4-amino-3,5-dinitrobenzenesulfonyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 4-amino-3,5-dinitrobenzenesulfonyl chloride(42760-43-0)
• EPA Substance Registry System: 4-amino-3,5-dinitrobenzenesulfonyl chloride(42760-43-0)

Safety Data

• Hazardous Substances Data: 42760-43-0(Hazardous Substances Data)

Upstream product

• 606-22-4 2,6-dinitroaniline 
• 38185-06-7 potassium 4-chloro-3,5-dinitrobenzene sulfonate 
• 90403-46-6 potassium 4-amino-3,5-dinitrobenzenesulfonate 
• 121-60-8 p-acetylaminobenzenesulfonyl chloride 
• 21208-62-8 ethyl 4-(chlorosulfonyl)phenylcarbamate 
• 35168-72-0 4-Chloro-3,5-dinitrobenzenesulphonyl Chloride 

Downstream Products

• 859032-72-7 5-methylsulfanyl-benzene-1,2,3-triyltriamine 
• 13279-51-1 3.5-Dinitro-sulfanilylhydrazid 
• 408340-26-1 3,4,5-triamino-thiophenol 

Relevant articles and documents

Synthesis of SMZ derivatives and investigation of effects on germination, root, and plant growth of Arabidopsis thaliana L.

A series of sulfonamide derivatives were synthesized by reactions with various functional groups containing benzenesulfonyl chlorides and aniline derivatives under different substitution reaction conditions. The structures of SMZ derivatives were confirmed with melting point, FT-IR, 1 H NMR, 13 C NMR, and LC-MS/MS techniques. In order to investigate the cytotoxic effects of these derivatives, we used a model plant species. The synthesized compounds (S1–S5) and sulfamethazine (SMZ) as a positive control were applied to Arabidopsis thaliana seeds. Our results indicated that S3 and S4 induced shorter roots and lower wet weight in plants. Plants treated with S2 and S5 showed no growth effects, similar to the untreated control group, while S1 slightly reduced root length and wet weight. These results suggest that S3 and the newly synthesized S4 derivatives have potential for use as herbicides since they possess cytotoxic effects on A. thaliana plants.

Discovery of a novel series of N-phenylindoline-5-sulfonamide derivatives as potent, selective, and orally bioavailable Acyl CoA:monoacylglycerol acyltransferase-2 inhibitors

Acyl CoA:monoacylglycerol acyltransferase-2 (MGAT2) has attracted interest as a novel target for the treatment of obesity and metabolic diseases. Starting from N-phenylbenzenesulfonamide derivative 1 with moderate potency for MGAT2 inhibition, we explored

The Preparation of Sodium 4-Amino-3-nitrobenzenesulfonate and Some Related Compounds

The sodium salt of 4-amino-3-nitrobenzenesulfonic acid (o-nitroaniline-p-sulfonic acid) has been prepared by the action of dilute sodium hydroxide solution on ethyl carbamate.Central to this synthesis is the finding that the N-ethoxycarbonyl group, when located ortho to a nitro group (but not to a bromo group), is readily removed by dilute sodium hydroxide solution.