160088-65-3

Basic information

• Product Name: N-{2,3-bisnitro-4-methylphenyl}acetamide
• Synonyms: N-{2,3-bisnitro-4-methylphenyl}acetamide
• CAS NO: 160088-65-3
• Molecular Formula: C₉H₉N₃O₅
• Molecular Weight: 239.18486
• Mol File: 160088-65-3.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-{2,3-bisnitro-4-methylphenyl}acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-{2,3-bisnitro-4-methylphenyl}acetamide(160088-65-3)
• EPA Substance Registry System: N-{2,3-bisnitro-4-methylphenyl}acetamide(160088-65-3)

Safety Data

• Hazardous Substances Data: 160088-65-3(Hazardous Substances Data)

Upstream product

• 2719-14-4 4-acetylamino-2-nitrotoluene 
• 7697-37-2 nitric acid 
• 7664-93-9 sulfuric acid 
• 70343-09-8 2,3-dinitro-4-methylaniline 
• 108-24-7 acetic anhydride 

Downstream Products

• 602-29-9 2,3,4-trinitrotoluene 
• 56433-00-2 3-chloro-2-nitrobenzyl bromide 
• 5367-26-0 3-chloro-2-nitrotoluene 
• 70343-09-8 2,3-dinitro-4-methylaniline 

Relevant articles and documents

Polyaza Heterocycles. Part 2. Nucleophilic Substitution of Halogens in Halogenoquinoxalinocinnolines

10-Chloroquinoxalinocinnoline readily undergoes methoxydechlorination when treated with sodium methoxide.The 1-, 2-, 3-, 4- and 9-chloro isomers are unreactive towards this reagent, but the 9,10-dichloro derivative undergoes substitution of both chlorines (the 10-position being much the more reactive).The 9- and 10-bromo analogues are both unreactive towards sodium methoxide, but the 9- and 10-fluoro analogues are both highly reactive, to the extent that it has not been possible even to isolate the 10-fluoro compound.Routes to 9- and 10-piperidinoquinoxalinocinnolines are described.