512773-83-0

Basic information

• Product Name: 4-amino-3-p-chIorophenoxy-2-p-chIorophenoxymethyI-10-methyl-7-nitropyrimido[1,2-a]indole
• Synonyms: 4-amino-3-p-chIorophenoxy-2-p-chIorophenoxymethyI-10-methyl-7-nitropyrimido[1,2-a]indole
• CAS NO: 512773-83-0
• Molecular Weight: 509.348
• Mol File: 512773-83-0.mol

Chemical Properties

• CAS DataBase Reference: 4-amino-3-p-chIorophenoxy-2-p-chIorophenoxymethyI-10-methyl-7-nitropyrimido[1,2-a]indole(CAS DataBase Reference)
• NIST Chemistry Reference: 4-amino-3-p-chIorophenoxy-2-p-chIorophenoxymethyI-10-methyl-7-nitropyrimido[1,2-a]indole(512773-83-0)
• EPA Substance Registry System: 4-amino-3-p-chIorophenoxy-2-p-chIorophenoxymethyI-10-methyl-7-nitropyrimido[1,2-a]indole(512773-83-0)

Safety Data

• Hazardous Substances Data: 512773-83-0(Hazardous Substances Data)

Upstream product

• 475641-18-0 1-methoxy-6-nitroindole-3-carbaldehyde 
• 354807-12-8 1-hydroxy-6-nitroindole 
• 125812-46-6 1-methoxy-6-nitroindole 
• 19727-83-4 6-nitroindoline 
• 496-15-1 1-indoline 
• 512773-79-4 4-amino-3-p-chlorophenoxy-2-p-chlorophenoxymethyl-7-nitropyrimido[1,2-a]indole-10-carbaldehyde 

Relevant articles and documents

Nucleophilic substitution reaction in indole chemistry: 1-methoxy-6-nitroindole-3-carbaldehyde as a versatile building block for 2,3,6-trisubstituted indoles

1-Methoxy-6-nitroindole-3-carbaldehyde is proved to be a versatile electrophile and reacts regioselectively at the 2-position with various types of nucleophiles providing 2,3,6-trisubstituted indole derivatives. The reaction is applicable for the preparation of a novel pyrimido[1,2-a]indole derivative.

Nucleophilic substitution reactions of 1-methoxy-6-nitroindole-3-carbaldehyde 1

1-Methoxy-6-nitroindole-3-carbaldehyde is proved to be a versatile substrate for the nucleophilic substitution reactions providing 2,3,6-trisubstituted indole derivatives. Preparation of a novel pyrimido[1,2-a]indole derivative is also reported.