14476-62-1

Basic information

• Product Name: Benzene, [(ethylthio)ethynyl]-
• CAS NO: 14476-62-1
• Molecular Formula: C10H10S
• Molecular Weight: 162.255
• Mol File: 14476-62-1.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: Benzene, [(ethylthio)ethynyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, [(ethylthio)ethynyl]-(14476-62-1)
• EPA Substance Registry System: Benzene, [(ethylthio)ethynyl]-(14476-62-1)

Safety Data

• Hazardous Substances Data: 14476-62-1(Hazardous Substances Data)

Upstream product

• 25445-77-6 4-phenyl-1,2,3-thiadiazole 
• 75-03-6 ethyl iodide 
• 925-90-6 ethylmagnesium bromide 
• 53646-00-7 4-phenyl-5-chloro-1,2,3-thiadiazole 
• 536-74-3 phenylacetylene 
• 75-08-1 ethanethiol 
• 33440-88-9 silver phenylacetylide 
• 2170-06-1 1-Phenyl-2-(trimethylsilyl)acetylene 
• 64846-61-3 phenylacetylenic zinc bromide 
• 352-93-2 diethyl sulphide 
• 1483-82-5 phenylethynyl chloride 
• 98-86-2 acetophenone 
• 10271-55-3 2-(ethylthio)-1-phenylethanone 
• 70-11-1 α-bromoacetophenone 

Downstream Products

• 36814-62-7 phenylethynylthioacetic acid methyl ester 
• 20890-79-3 (Z)-β-(ethylthio)styrene 
• 65832-84-0 1-ethylsulfinyl-2-phenylacetylene 
• 338451-17-5 Toluene-4-sulfonic acid (Z)-1-methylsulfanyl-2-phenyl-vinyl ester 
• 54588-90-8 (E)-1-methoxy-4-(1-phenylprop-1-en-1-yl)benzene 
• 54588-89-5 (Z)-1-methoxy-4-(1-phenylprop-1-en-1-yl)benzene 
• 180062-59-3 (Z)-1-(4-methoxylphenyl)-2-phenylprop-1-ene 
• 1562258-07-4 C₁₆H₂₃BO₂S 
• 1562258-71-2 C₁₆H₂₃BO₂S 

Relevant articles and documents

Radical-mediated sulfonyl alkynylation, allylation, and cyanation of propellane

Bicyclo[1.1.1]pentane (BCP) is widely applied as the bioisostere for aryl, internal alkynes, andtert-butyl groups in medicinal chemistry. We herein disclose an efficient and practical preparation of sulfonyl alkynyl/allyl/cyano-substituted BCP derivatives

N-Alkynylthio Phthalimide: A Shelf-Stable Alkynylthio Transfer Reagent for the Synthesis of Alkynyl Thioethers

A new kind of electrophilic alkynylthiolating reagent, called N-alkynylthio phthalimide, is designed and synthesized herein. This electrophilic sulfenylating reagent can be easily prepared in three steps from commercially available phthalimide and corresp

A Highly Regio- and Stereoselective Syntheses of α-Halo Enamides, Vinyl Thioethers, and Vinyl Ethers with Aqueous Hydrogen Halide in Two-Phase Systems

A metal-free regio- and stereoselective method is achieved for the preparation of (E)-configured α-halo enamides, vinyl thioethers, and vinyl ethers using aqueous HX (X = F, Cl, Br, I), which features high functional group compatibility and regio- and stereoselectivity, mild conditions, high efficiency, and rapid transformation. Additionally, the isomers could be yielded readily from the (E)-configured α-halo enamides via photocatalysis or under Sonogashira coupling conditions.