62876-66-8

Basic information

• Product Name: Benzoic acid, 5-(dimethylamino)-2-nitro-
• CAS NO: 62876-66-8
• Molecular Formula: C9H10N2O4
• Molecular Weight: 210.189
• Mol File: 62876-66-8.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 5-(dimethylamino)-2-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 5-(dimethylamino)-2-nitro-(62876-66-8)
• EPA Substance Registry System: Benzoic acid, 5-(dimethylamino)-2-nitro-(62876-66-8)

Safety Data

• Hazardous Substances Data: 62876-66-8(Hazardous Substances Data)

Upstream product

• 2516-95-2 5-chloro-2-nitrobenzoic acid 
• 124-40-3 dimethyl amine 
• 50-00-0 formaldehyd 
• 13280-60-9 5-amino-2-nitrobenzoic acid 

Downstream Products

• 1140-50-7 3-(N,N-dimethylamino)-carbazole 
• 20129-87-7 2-amino-5-dimethylaminobenzoic acid 
• 749863-29-4 methyl 5-(dimethylamino)-2-nitrobenzoate 

Relevant articles and documents

Tuning a robust system: N,O zinc guanidine catalysts for the ROP of lactide

Non-toxic, highly active and robust complexes are the holy grail as ideal green catalysts for the polymerisation of biorenewable and biodegradable polylactide. Four new zinc guanidine complexes [ZnCl2(TMG4NMe2asme)], [ZnCl2(TMG5Clasme)], [ZnCl2(TMG5Measme)] and [ZnCl2(TMG5NMe2asme)] with different electron-donating and electron-withdrawing groups on the ligand's aromatic backbone have been synthesised. Ligands are derived from low-cost commercially available compounds and have been converted by a three- or four-step synthesis process into the desired ligand in good yields. The compounds have been fully characterised and tested in the ROP of rac-LA under industrially relevant conditions. The complexes are based on the recently published structure [ZnCl2(TMGasme)] which has shown high activity in the polymerisation of lactide at 150 °C. Different substituents in the para-position of the guanidine moiety significantly increase the polymerisation rate whereas positioning substituents in the meta-position causes no change in the reaction rate. With molecular weights over 71000 g mol-1 being achievable, the best system produces polymers for multiple industrial applications and its polymerisation rate approaches that of Sn(Oct)2. The robust systems are able to polymerise non-purified lactide. The initiation of the polymerisation is suggested to occur due to impurities in the monomer.

DIHYDROOROTATE DEHYDROGENASE AS ANTIFUNGAL DRUG TARGET AND QUINAZOLINONE-BASED INHIBITORS THEREOF

A method of identifying an antifungal agent which targets a DHODH protein (alias PyrE, dihydroorotate dehydrogenase, EC: 1.3.99.11) of a fungus comprising contacting a candidate substance with a fungal DHODH protein and determining whether the candidate s

PROCESS FOR PRODUCING PHENYLALANINE DERIVATIVE HAVING QUINAZOLINEDIONE SKELETON AND INTERMEDIATE FOR THE SAME

The present invention provides a method for producing a phenylalanine derivative(s) having a quinazolinedione ring of formula (5), including steps comprising of:reacting an acylphenylalanine derivative(s) of formula (1) with a carbonyl group-introducing r