17357-39-0

Basic information

• Product Name: S-(p-tolyl) furan-2-carbothioate
• Synonyms: S-(p-tolyl) furan-2-carbothioate
• CAS NO: 17357-39-0
• Molecular Weight: 218.276
• Mol File: 17357-39-0.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: S-(p-tolyl) furan-2-carbothioate(CAS DataBase Reference)
• NIST Chemistry Reference: S-(p-tolyl) furan-2-carbothioate(17357-39-0)
• EPA Substance Registry System: S-(p-tolyl) furan-2-carbothioate(17357-39-0)

Safety Data

• Hazardous Substances Data: 17357-39-0(Hazardous Substances Data)

Upstream product

• 527-69-5 2-furancarbonyl chloride 
• 106-45-6 para-thiocresol 
• 609-38-1 furan-2-carboxylic acid amide 
• 13331-23-2 fur-2-ylboronic acid 
• 98-59-9 p-toluenesulfonyl chloride 
• 13939-06-5 molybdenum hexacarbonyl 
• 88-14-2 2-furanoic acid 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 103-19-5 di(p-tolyl) disulfide 
• 144223-33-6 2-furoyl-1H-1,2,3-benzotriazole 

Downstream Products

• 1173164-15-2 C₂₀H₂₄O₂S 
• 1173163-83-1 C₂₀H₂₄O₂S 
• 216453-11-1 p-methylphenyl dithio-2-furoate 

Relevant articles and documents

Method for synthesizing thioester through cross-coupling of visible light-catalyzed sodium sulfinate and acyl chloride

The method takes sodium sulfinate and acyl chloride as raw materials and utilizes 2, 6 - dimethyl -1, 4 - dihydro -3, 5 - pyridine dicarboxylic acid diethyl ester and an organic alkali catalytic system to cross-couple sulfur radicals and acyl radicals und

Na2CO3-promoted thioesterification via N–C bond cleavage of amides to construct thioester derivatives

A mild, efficient, and transition-metal-free catalytic strategy is developed to construct thioesters via selective N–C bond cleavage of Boc2-activated primary amides. This strategy is successfully carried out with stoichiometric Na2C

Visible-Light-Promoted Thiyl Radical Generation from Sodium Sulfinates: A Radical-Radical Coupling to Thioesters

A convenient visible-light photoredox catalysis has been developed for the synthesis of thioesters from two readily available starting materials: acid chlorides and sodium sulfinates. The facile generation of acyl radical species under the visible light photoredox conditions allows the formation of thiyl radical species from sodium sulfinates via multiple single electron transfer reactions, where the final acyl radical-thiyl radical coupling has been accomplished. The direct radical-radical coupling strategy offers a mild and controlled photochemical approach to important synthetic building blocks such as thioesters.