165615-26-9

Basic information

• Product Name: 1-<1-(benzenesulfonyl)pyrrol-3-yl>ethanol
• Synonyms: 1-<1-(benzenesulfonyl)pyrrol-3-yl>ethanol
• CAS NO: 165615-26-9
• Molecular Weight: 251.306
• Mol File: 165615-26-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-<1-(benzenesulfonyl)pyrrol-3-yl>ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-<1-(benzenesulfonyl)pyrrol-3-yl>ethanol(165615-26-9)
• EPA Substance Registry System: 1-<1-(benzenesulfonyl)pyrrol-3-yl>ethanol(165615-26-9)

Safety Data

• Hazardous Substances Data: 165615-26-9(Hazardous Substances Data)

Upstream product

• 16881-77-9 (dimethoxy)methylsilane 
• 81453-98-7 3-acetyl-1-(phenylsulfonyl)pyrrole 
• 1165952-91-9 cyclohexa-1,3-diene 
• 16851-82-4 N-phenylsulfonylpyrrole 

Downstream Products

• 88075-95-0 1-(phenylsulfonyl)-1H-pyrrole-3-carbaldehyde 
• 422511-37-3 4,8-dimethyl-1-(phenylsulfonyl)-1H-furo[3,4-f]indole-5,7-dione 
• 422511-36-2 1-[1-benzenesulfonyl-2-(1-hydroxy-ethyl)-1H-pyrrol-3-yl]-ethanone 
• 130103-56-9 dimethyl 4,7-dimethyl-1-(phenylsulfonyl)-1H-indole-5,6-dicarboxylate 
• 586958-77-2 1-[1-(phenylsulfonyl)-1H-pyrrol-3-yl]-ethyl-2H-1,2,3-benzotriazole 

Relevant articles and documents

Benzannulation of 3-substituted pyrroles to indoles

In a new general indole synthesis, the anion derived from benzotriazolyl derivative 5b underwent regioselective 1,4-addition to various α,β-unsaturated ketones; subsequent acid-catalyzed cyclization formed the corresponding indoles 1a-f.

Synthesis and Diels-Alder reactions of the furo[3,4-b]pyrrole ring system. A new indole ring synthesis

The previously unknown furo[3,4-b]pyrrole ring system has been synthesized from the appropriate pyrrolo hydroxyketones by acid-catalyzed cyclodehydration. Diels-Alder reactions of these furo[3,4-b]pyrroles affords a new synthesis of indoles.

1-(BENZENESULFONYL)PYRROLE-3-CARBOXALDEHYDE

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