643735-26-6

Basic information

• Product Name: 4,7-DIMETHYL-10-P-TOLYL-9,10-DIHYDRO-4H-2-OXA-4,10-DIAZA-BENZO[F]AZULENE-1,3-DIONE
• Synonyms: 4,7-DIMETHYL-10-P-TOLYL-9,10-DIHYDRO-4H-2-OXA-4,10-DIAZA-BENZO[F]AZULENE-1,3-DIONE
• CAS NO: 643735-26-6
• Molecular Formula: C20H18N2O3
• Molecular Weight: 0
• Mol File: 643735-26-6.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4,7-DIMETHYL-10-P-TOLYL-9,10-DIHYDRO-4H-2-OXA-4,10-DIAZA-BENZO[F]AZULENE-1,3-DIONE(CAS DataBase Reference)
• NIST Chemistry Reference: 4,7-DIMETHYL-10-P-TOLYL-9,10-DIHYDRO-4H-2-OXA-4,10-DIAZA-BENZO[F]AZULENE-1,3-DIONE(643735-26-6)
• EPA Substance Registry System: 4,7-DIMETHYL-10-P-TOLYL-9,10-DIHYDRO-4H-2-OXA-4,10-DIAZA-BENZO[F]AZULENE-1,3-DIONE(643735-26-6)

Safety Data

• Hazardous Substances Data: 643735-26-6(Hazardous Substances Data)

Upstream product

• 79-37-8 oxalyl dichloride 
• 2739-04-0 N-methyl-N-(4-methylphenyl)formamide 

Relevant articles and documents

The surprising nucleophilic addition of aminochlorocarbenes to diethyl acetylenedicarboxylate and to oxalyl chloride: Quinolines and benzo[1,4]diazepines from N-alkylformanilides and oxalyl chloride in the presence of Huenig's base

Vilsmeier reagents derived from N-methylformanilides undergo ready deprotonation with Huenig's base. In xylene, the derived nucleophilic arylaminochlorocarbenes bearing 4-methyl- and 4-methoxy-substituents react with acetylenedicarboxylates to give 2-(2-c