90234-69-8

Basic information

• Product Name: 1H-Indole-1-carboximidoyl chloride, 2,3-dihydro-N-(4-nitrobenzoyl)-
• CAS NO: 90234-69-8
• Molecular Formula: C16H12ClN3O3
• Molecular Weight: 329.743
• Mol File: 90234-69-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1H-Indole-1-carboximidoyl chloride, 2,3-dihydro-N-(4-nitrobenzoyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indole-1-carboximidoyl chloride, 2,3-dihydro-N-(4-nitrobenzoyl)-(90234-69-8)
• EPA Substance Registry System: 1H-Indole-1-carboximidoyl chloride, 2,3-dihydro-N-(4-nitrobenzoyl)-(90234-69-8)

Safety Data

• Hazardous Substances Data: 90234-69-8(Hazardous Substances Data)

Upstream product

• 90036-14-9 N-cyano-indoline 
• 122-04-3 4-nitro-benzoyl chloride 

Downstream Products

• 90235-01-1 N-(4-Nitrobenzoyl)-1-indolinthiocarboximidsaeure-4-methylphenylester 
• 90235-09-9 N-Butyl-N'-(4-nitrobenzoyl)-2-isoindolincarboxamidin 
• 90234-91-6 N-(4-Nitrobenzoyl)-1-indolincarboxamid 
• 90235-05-5 S-(Diethylthiocarbamoyl)-N-(4-nitrobenzoyl)-1-indolinthiocarboximidsaeure 
• 90235-08-8 N-(4-Nitrobenzoyl)-1-indolincarboximidsaeure-morpholid 

Relevant articles and documents

Synthesis of New Carboximidoyl Chlorides and Their Reaction with Nucleophiles

One-step reactions of N,N-dialkylcyanamides 1a-c and dicarbonitriles 1d, e with organic acyl chlorides and with 2-chloro-1,1-dicyanoethylenes easily lead to the N-acyl-substituted carboximidoyl chlorides 2a-k and biscarboximidoyl chlorides 2l-v, respectively.The substituents in the α-position of the chlorocarbonyl group have a strong influence on the stability of the reaction products.The carboximidoyl chlorides 2a, f, o, and u react with O-nucleophiles (H2O, alcohols, phenols), S-nucleophiles (dithiocarbamates, thiophenols), and N-nucleophiles (NH3, aliphatic and aromatic amines) to give a variety of products.