39689-09-3

Basic information

• Product Name: 2-Furancarboxaldehyde, 5-(phenylsulfonyl)-
• CAS NO: 39689-09-3
• Molecular Formula: C11H8O4S
• Molecular Weight: 236.248
• Mol File: 39689-09-3.mol

Chemical Properties

• CAS DataBase Reference: 2-Furancarboxaldehyde, 5-(phenylsulfonyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Furancarboxaldehyde, 5-(phenylsulfonyl)-(39689-09-3)
• EPA Substance Registry System: 2-Furancarboxaldehyde, 5-(phenylsulfonyl)-(39689-09-3)

Safety Data

• Hazardous Substances Data: 39689-09-3(Hazardous Substances Data)

Upstream product

• 930-69-8 sodium thiophenolate 
• 698-63-5 5-nitrofurane-2-carboxaldehyde 
• 27329-70-0 5-formylfurane-2-boronic acid 
• 98-09-9 benzenesulfonyl chloride 
• 39689-03-7 5-(phenylsulfanyl)-2-furaldehyde 

Downstream Products

• 95457-68-4 2-Benzenesulfonyl-5-((E)-2-nitro-vinyl)-furan 
• 106240-57-7 5-phenylsulfonyl-2-furonitrile 
• 98387-07-6 2-[(5-Benzenesulfonyl-furan-2-yl)-(4-phenyl-piperazin-1-yl)-methyl]-malonic acid diethyl ester 
• 98387-14-5 C₃₁H₃₄N₄O₃S 
• 98387-06-5 2-[(5-Benzenesulfonyl-furan-2-yl)-morpholin-4-yl-methyl]-malonic acid diethyl ester 
• 98387-05-4 2-[(5-Benzenesulfonyl-furan-2-yl)-piperidin-1-yl-methyl]-malonic acid diethyl ester 
• 98387-08-7 2-[(5-Benzenesulfonyl-furan-2-yl)-pyrrolidin-1-yl-methyl]-malonic acid diethyl ester 
• 95685-24-8 (Z)-2-Benzenesulfonyl-3-(5-morpholin-4-yl-furan-2-yl)-acrylonitrile 
• 95685-28-2 (Z)-2-Benzoyl-3-(5-morpholin-4-yl-furan-2-yl)-acrylonitrile 
• 95685-22-6 (Z)-2-Benzenesulfonyl-3-(5-piperidin-1-yl-furan-2-yl)-acrylonitrile 
• 95685-26-0 (Z)-2-Benzoyl-3-(5-piperidin-1-yl-furan-2-yl)-acrylonitrile 
• 95685-23-7 (Z)-2-Benzenesulfonyl-3-(5-pyrrolidin-1-yl-furan-2-yl)-acrylonitrile 
• 95685-27-1 (Z)-2-Benzoyl-3-(5-pyrrolidin-1-yl-furan-2-yl)-acrylonitrile 
• 76500-26-0 methyl 2-cyano-3-(5-(N-benzyl)piperazino-2-furyl)acrylate 

Relevant articles and documents

Application of furyl-stabilized sulfur ylides to a concise synthesis of 8a-epi-swainsonine

The total synthesis of 8a-epi-swainsonine has been achieved in 20% overall yield from R-glyceraldehyde dimethylacetonide 3 through epoxidation with the achiral furyl-substituted sulfonium ylide 2d as one of the key steps. The Royal Society of Chemistry.

Unsymmetrical diaryl sulfones through palladium-catalyzed coupling of aryl boronic acids and arylsulfonyl chlorides

A simple and efficient method for the synthesis of unsymmetrical diaryl sulfones using the palladium-catalyzed coupling of aryl boronic acids and arylsulfonyl chlorides has been developed. High product yields, a short reaction time, and mild reaction conditions are important features of this method.

Synthesis of sulfone-substituted furan chromophores with high molecular hyperppolarizability

A series of sulfone-substituted furan chromophores were synthesized which showed high molecular hyperpolarizabilities as measured by solvatochromism, and good transparency in the visible region.