147295-24-7

Basic information

• Product Name: 2,5-dimethyl-1-(phenylsulfonyl)-1H-pyrrole-3,4-dicarbaldehyde
• CAS NO: 147295-24-7
• Molecular Weight: 291.328
• Mol File: 147295-24-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2,5-dimethyl-1-(phenylsulfonyl)-1H-pyrrole-3,4-dicarbaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-dimethyl-1-(phenylsulfonyl)-1H-pyrrole-3,4-dicarbaldehyde(147295-24-7)
• EPA Substance Registry System: 2,5-dimethyl-1-(phenylsulfonyl)-1H-pyrrole-3,4-dicarbaldehyde(147295-24-7)

Safety Data

• Hazardous Substances Data: 147295-24-7(Hazardous Substances Data)

Upstream product

• 56139-74-3 2,5-dimethyl-1H-pyrrole-3,4-dicarbaldehyde 
• 98-09-9 benzenesulfonyl chloride 

Downstream Products

• 856252-06-7 (3E,4E)-dimethyl 3,3'-(2,5-dimethyl-1-(phenylsulfonyl)-1H-pyrrole-3,4-diyl)diacrylate 
• 129661-79-6 tetraethyl <(1-phenylsulfonyl-2,5-dibromomethyl-3,4-pyrrolediyl)dimethylene>bis(propanedioate) 
• 129661-78-5 tetraethyl <(1-phenylsulfonyl-2,5-dimethyl-3,4-pyrrolediyl)dimethylene>bis(propanedioate) 

Relevant articles and documents

Synthesis of substituted carbazoles via electrocyclization of in situ generated enamines from 1-phenylsulfonyl-2/(3)-methyl-3/(2)-vinylindoles and DMF·DMA/DMA·DMA

Interaction of 2/(3)-methyl-3/(2)-vinylindoles and DMF·DMA/DMA·DMA at 110 °C led to the in situ generation of enamines, which on concurrent electrocyclization followed by subsequent aromatization afforded substituted carbazoles.