1210-97-5

Basic information

• Product Name: Benzoic acid, 4-(acetyloxy)-3-nitro-
• CAS NO: 1210-97-5
• Molecular Formula: C9H7NO6
• Molecular Weight: 225.158
• Mol File: 1210-97-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 4-(acetyloxy)-3-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 4-(acetyloxy)-3-nitro-(1210-97-5)
• EPA Substance Registry System: Benzoic acid, 4-(acetyloxy)-3-nitro-(1210-97-5)

Safety Data

• Hazardous Substances Data: 1210-97-5(Hazardous Substances Data)

Upstream product

• 616-82-0 3-nitro-4-hydroxybenzoic acid 
• 108-24-7 acetic anhydride 

Downstream Products

• 616-82-0 3-nitro-4-hydroxybenzoic acid 
• 52955-54-1 4-acetoxy-3-nitrobenzoate 
• 64-19-7 acetic acid 

Relevant articles and documents

BICYCLIC HETEROCYCLIC DERIVATIVE

The present invention relates to a compound of the following formula (I) or a pharmaceutically acceptable salt thereof, being useful as a renin inhibitor. [wherein R1a is halogen, etc.; R1m is H, etc.; G1 is -N(R1b/s

Synthesis and structure-activity relationship of diarylamide derivatives as selective inhibitors of the proliferation of human coronary artery smooth muscle cells

A series of diarylamide derivatives were synthesized and evaluated for their inhibitory activities against human coronary artery smooth muscle cells (SMCs) and human coronary artery endothelial cells (ECs). Compound 2w was superior to the lead compound, Tranilast, in terms of the potency of the activity and cell selectivity.

Contrasting Behaviors in the Cleavage of Aryl Alkanoates by α- and β-Cyclodextrins in Basic Aqueous Solution

The kinetics of ester cleavage of 4-carboxy-2-nitrophenyl alkanoates (C2, C4, C6, C7, C8) in aqueous base containing α- or β-cyclodextrin (α- or β-CD) indicate that for the three longer esters there are processes involving two CD molecules which are quite distinct: with α-CD a 2:1 binding leads to inhibition; with β-CD a second-order process provides catalysis.