143484-14-4

Basic information

• Product Name: Benzoic acid, 3-[2-(dimethylamino)ethenyl]-4-nitro-, methyl ester
• CAS NO: 143484-14-4
• Molecular Formula: C12H14N2O4
• Molecular Weight: 250.254
• Mol File: 143484-14-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 3-[2-(dimethylamino)ethenyl]-4-nitro-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 3-[2-(dimethylamino)ethenyl]-4-nitro-, methyl ester(143484-14-4)
• EPA Substance Registry System: Benzoic acid, 3-[2-(dimethylamino)ethenyl]-4-nitro-, methyl ester(143484-14-4)

Safety Data

• Hazardous Substances Data: 143484-14-4(Hazardous Substances Data)

Upstream product

• 3113-71-1 3-methyl-4-nitrobenzoic acid 
• 4637-24-5 N,N-dimethyl-formamide dimethyl acetal 
• 24078-21-5 methyl 3-methyl-4-nitrobenzoate 

Downstream Products

• 850074-03-2 benzo[b]thiophene-2,5-dicarboxylic acid 2-hydroxyamide 5-(2-methoxy-benzylamide) 
• 850074-02-1 2-trityloxycarbamoyl-benzo[b]thiophene-5-carboxylic acid 
• 850073-98-2 benzo[b]thiophene-2,5-dicarboxylic acid 5-methyl ester 
• 850073-97-1 benzo[b]thiophene-2,5-dicarboxylic acid 2-tert-butyl ester 5-methyl ester 
• 438003-11-3 methyl 4-nitro-3-(2-oxopentyl)benzoate 
• 148625-35-8 methyl 3-formyl-4-nitrobenzoate 
• 1011-65-0 5-methoxycarbonylindole 

Relevant articles and documents

Synthesis and biological activities of novel indole derivatives as potent and selective PPARγ modulators

Starting from the structure of Telmisartan, a new series of potent and selective PPARγ modulators was identified. The synthesis, in vitro and in vivo evaluation of the most potent compounds are reported and the X-ray structure of compound 7b bound to the PPARγ ligand binding domain is described.

THIOPHENE AND BENZOTHIOPHENE HYDROXAMIC ACID DERIVATIVES

The present invention relates to a novel class of hydroxamic acid derivatives having a benzothiophene or thiophene backbone. The hydroxamic acid compounds can be used to treat cancer. The hydroxamic acid compounds can also inhibit historic deacetylase and