1542548-47-9

Basic information

• Product Name: 1-methyl-5-[(2-nitrophenyl)amino]-1H-pyrazole-4-carbaldehyde
• Synonyms: 1-methyl-5-[(2-nitrophenyl)amino]-1H-pyrazole-4-carbaldehyde
• CAS NO: 1542548-47-9
• Molecular Weight: 246.225
• Mol File: 1542548-47-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-methyl-5-[(2-nitrophenyl)amino]-1H-pyrazole-4-carbaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 1-methyl-5-[(2-nitrophenyl)amino]-1H-pyrazole-4-carbaldehyde(1542548-47-9)
• EPA Substance Registry System: 1-methyl-5-[(2-nitrophenyl)amino]-1H-pyrazole-4-carbaldehyde(1542548-47-9)

Safety Data

• Hazardous Substances Data: 1542548-47-9(Hazardous Substances Data)

Upstream product

• 117007-77-9 5-chloro-1-methyl-1H-pyrazole-4-carbaldehyde 
• 88-74-4 2-nitro-aniline 

Downstream Products

• 479234-83-8 1-methyl-1,4,5,10-tetrahydrobenzo[b]pyrazolo[3,4-e][1,4]diazepine 
• 479234-64-5 (4-(aminomethyl)-3-methylphenyl)(1-methyl-3a,4,10,10a-tetrahydrobenzo[b]pyrazolo[3,4-e][1,4]diazepin-5(1H)-yl)methanone 
• 479234-62-3 2-methyl-4-(1-methyl-1,3a,4,5,10,10a-hexahydrobenzo[b]-pyrazolo[3,4-e][1,4]diazepine-5-carbonyl)benzonitrile 
• 847375-16-0 WAY-267464 

Relevant articles and documents

THERAPEUTIC COMPOUNDS AND COMPOSITIONS FOR TREATING SOCIAL DISORDERS AND SUBSTANCE USE DISORDERS

Disclosed herein are compounds, compositions and methods for the treatment of neurological, psychiatric disorders which are characterised by a fundamental disruption of social behaviour, and substance use disorders. In particular, disclosed herein are com

Synthesis of biologically active seven-membered-ring heterocycles

Seven-membered rings that contain one or more heteroatoms are interesting motifs for organic synthesis. In addition to their synthetic interest, they play an important role in industrial and pharmaceutical chemistry with generally increased central nervous system activity when flanked by aromatic rings. Herein we report a brief summary of some key methods of preparation for seven-membered-ring heterocycles and how they have been applied to the synthesis of commercially desirable products. We then detail new methods that we have developed for the synthesis of biologically active compounds containing this motif. Georg Thieme Verlag Stuttgart New York.