91538-60-2

Basic information

• Product Name: N-(2-FORMYL-4-NITROPHENYL)ACETAMIDE
• Synonyms: N-(2-FORMYL-4-NITROPHENYL)ACETAMIDE
• CAS NO: 91538-60-2
• Molecular Formula: C₉H₈N₂O₄
• Molecular Weight: 0
• Mol File: 91538-60-2.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-(2-FORMYL-4-NITROPHENYL)ACETAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-FORMYL-4-NITROPHENYL)ACETAMIDE(91538-60-2)
• EPA Substance Registry System: N-(2-FORMYL-4-NITROPHENYL)ACETAMIDE(91538-60-2)

Safety Data

• Hazardous Substances Data: 91538-60-2(Hazardous Substances Data)

Upstream product

• 13493-47-5 N-(2-formylphenyl)acetamide 
• 55857-35-7 (E)-N-(2-aminobenzylidene)-4-methylaniline 
• 142598-80-9 acetic acid-[2-((E)-p-tolylimino-methyl)-anilide] 
• 5344-90-1 2-Aminobenzyl alcohol 
• 20939-77-9 2-acetamidobenzyl alcohol 

Downstream Products

• 1003024-71-2 methyl 3-(2-acetamido-5-nitrophenyl)-3-hydroxy-2-methylenepropanoate 
• 3558-18-7 5-nitro-N-acetylanthranilic acid 
• 861222-14-2 acetic acid-(2-hydroxymethyl-4-nitro-anilide) 
• 85870-48-0 1,2-dihydro-6-nitro-2-oxo-3-quinolinecarboxylic acid ethyl ester 
• 91538-58-8 2-chloro-6-nitro-3-quinolinecarboxylic acid ethyl ester 
• 85870-49-1 1,2-dihydro-6-nitro-2-oxo-3-quinolinecarboxylic acid 
• 85870-50-4 6-amino-1,2-dihydro-2-oxo-3-quinolinecarboxylic acid 
• 21872-92-4 6-amino-3-quinolinecarboxylic acid ethyl ester 
• 248937-21-5 (S,R)-2-[(2-hydroxy-1-phenylethyl)amino]-2-(2-iodo-5-nitrophenyl)ethanenitrile 
• 56008-60-7 2-iodo-5-nitrobenzaldehyde 
• 56008-61-8 2-amino-5-nitrobenzaldehyde 
• 64495-55-2 6-nitroquinolin-2-ol 
• 77242-30-9 (2-amino-5-nitrophenyl)methanol 
• 616-79-5 2-amino-5-nitro-benzoic acid 

Relevant articles and documents

NOVEL IMIDAZO-PYRAZINE DERIVATIVES

The invention provides novel imidazo-pyrazine derivatives having the general formula (I), and pharmaceutically acceptable salts thereof, wherein X, m, n, and R1to R3 are as described herein: formula (I). Further provided are pharmace

A simple and efficient diastereoselective Strecker synthesis of optically pure α-arylglycines

A simple and economical method for the synthesis of highly functionalised α-amino nitriles, precursors to α-arylglycines with high optical purity is reported. For this purpose, (R) or (S)-2-amino-2- phenylethanol were used as chiral auxiliaries in a 1,3 Strecker reaction. Reactions were studied with a broad range of reagent systems for the generation of cyano nucleophile. Methodology has been extended for the synthesis of (S)-α-(2-iodo-5-nitrophenyl)glycine, (S)-α-(4- methoxyphenyl)glycine and (R)-β-(4-methoxyphenyl)alanine.