10524-65-9

Basic information

• Product Name: 1H-Pyrrole, 1,3-dimethyl-
• CAS NO: 10524-65-9
• Molecular Formula: C6H9N
• Molecular Weight: 95.1442
• Mol File: 10524-65-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1H-Pyrrole, 1,3-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrole, 1,3-dimethyl-(10524-65-9)
• EPA Substance Registry System: 1H-Pyrrole, 1,3-dimethyl-(10524-65-9)

Safety Data

• Hazardous Substances Data: 10524-65-9(Hazardous Substances Data)

Upstream product

• 116773-34-3 1,1,4-trimethyl-5-phenyl-1,5-diazapentadiene 
• 116773-21-8 1,1,3-trimethyl-5-phenyl-1,5-diazapentadiene 

Downstream Products

• 20116-65-8 dimethyl 4-methylphthalate 
• 74986-25-7 trimethyl 5-methylbenzene-1,2,3-tricarboxylate 
• 74986-16-6 tetramethyl 3a,7a-dihydro-1,6-dimethylindole-2,3,3a,4-tetracarboxylate 
• 23893-69-8 trimethyl 1-methyl-1H-pyrrole-2,3,4-tricarboxylate 
• 74985-94-7 dimethyl (Z)-1,3-dimethyl-2-pyrrolyl-2-butenedioate 
• 73529-28-9 dimethyl 1-methyl-1H-pyrrole-3,4-dicarboxylate 

Relevant articles and documents

Thermolysis of Polyazapentadienes. Part 8. The formation of Pyrroles from 1,1-Dialkyl-5-aryl-1,5-diazapentadienes

Flash vacuum pyrolysis of the 1,5-diazapentadienes (4)-(10) gave moderate yields of pyrroles together with quinolines, formed by electrocyclic ring closure with elimination.The pyrroles were formed by hydrogen transfer from an N-alkyl group, followed by cyclisation and final aromatisation of the resulting dihydropyrrole intermediate by free-radical cleavage.The mechanism of the hydrogen transfer and cyclisation is not known with certainty, but may involve diradicals or 1,5-dipolar intermediates.