24182-83-0

Basic information

• Product Name: 1-methyl-4-{[(Z)-2-phenylethenyl]sulfanyl}benzene
• CAS NO: 24182-83-0
• Molecular Formula: C₁₅H₁₄S
• Molecular Weight: 226.3367
• Mol File: 24182-83-0.mol
• Article Data: 38

Chemical Properties

• Boiling Point: 362.3°C at 760 mmHg
• Flash Point: 168°C
• Density: 1.09g/cm³
• Vapor Pressure: 4.07E-05mmHg at 25°C
• Refractive Index: 1.627
• CAS DataBase Reference: 1-methyl-4-{[(Z)-2-phenylethenyl]sulfanyl}benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-methyl-4-{[(Z)-2-phenylethenyl]sulfanyl}benzene(24182-83-0)
• EPA Substance Registry System: 1-methyl-4-{[(Z)-2-phenylethenyl]sulfanyl}benzene(24182-83-0)

Safety Data

• Hazardous Substances Data: 24182-83-0(Hazardous Substances Data)

Usage

Physical state

colorless liquid
Thioanisole is a colorless liquid, meaning it does not have any color and flows like a liquid at room temperature.

Odor

sweet, aromatic
Thioanisole has a sweet and aromatic odor, which contributes to its use as a flavor and fragrance ingredient.

Common uses

flavor and fragrance ingredient, solvent, synthesis of organic compounds, and reagent in organic chemistry reactions
Thioanisole is commonly used in various applications, such as a flavor and fragrance ingredient in perfumes, dyes, and pharmaceuticals, as a solvent, in the synthesis of organic compounds, and as a reagent in organic chemistry reactions.

Hazardous properties

flammable, potentially hazardous
Thioanisole is a flammable and potentially hazardous substance, which means it should be handled with care to avoid accidents and ensure safety.

Upstream product

• 10486-08-5 sodium p-thiocresolate 
• 536-74-3 phenylacetylene 
• 141-52-6 sodium ethanolate 
• 106-45-6 para-thiocresol 
• 103-19-5 di(p-tolyl) disulfide 
• 1576-35-8 toluene-4-sulfonic acid hydrazide 
• 933-00-6 p-methylbenzenesulfenyl chloride 
• 588-72-7 [(E)-2-bromoethenyl]benzene 
• 2943-42-2 di(4-methyl)phenylthiosulfonate 
• 6783-05-7 trans-2-phenylvinylboronic acid 
• 100-42-5 styrene 
• 934-72-5 Methyl p-tolyl sulfoxide 
• 63707-12-0 1-(4-methylphenylsulfanyl)-2-phenylethyne 
• 38986-89-9 trans-cinnamoyl fluoride 

Downstream Products

• 41103-85-9 (Z)-1-methyl-4-(styrylsulfinyl)benzene 
• 16212-08-1 (Z)-1-methyl-4-(styrylsulfonyl)benzene 
• 41103-85-9 (E)-1-methyl-4-(styrylsulfinyl)benzene 
• 16212-08-1 1-methyl-4-[(E)-2-phenylethenesulfonyl]benzene 
• 1068599-48-3 CH₃C₆H₄SCHCH₂C₆H₅BO₂C₆H₄ 
• 156575-59-6 2-(2-phenylethyl)benzo-1,3,2-dioxaborole 
• 174090-36-9 4,4,5,5-tetramethyl-2-(1-phenyl-ethyl)-[1,3,2]dioxaborolane 
• 165904-22-3 4,4,5,5-tetramethyl-2-phenethyl-1,3,2-dioxaborolane 
• 1068599-50-7 CH₃C₆H₄SCH₂CHBO₂C₆H₄C₆H₅ 
• 156575-60-9 2-(1-phenyl-ethyl)-benzo[1,3,2]dioxaborole 
• 19062-76-1 (1-phenyl-2-tosylethyl)-(p-tolyl)sulfane 
• 211929-53-2 (2-tosylethane-1,1-diyl)dibenzene 

Relevant articles and documents

Base-Promoted Stereoselective Hydrogenation of Ynamides with Sulfonyl Hydrazide to Give Z-Enamides

A base-mediated semihydrogenation of ynamides using p-toluenesulfonyl hydrazide as an inexpensive and easy-to-handle hydrogen donor is reported. This transition-metal-free protocol avoids overhydrogenation and reduction of other functional groups, generating the thermodynamically unfavorable Z-enamides exclusively.

Nickel-Catalyzed Decarbonylative Thioetherification of Acyl Fluorides via C-F Bond Activation

Nickel-catalyzed decarbonylative thioetherification of acyl fluorides has been developed. This transformation allows an array of acyl fluorides to react with thiophenols. A wide range of functional groups are well tolerated and the corresponding sulfides can be obtained in good to excellent yields. This protocol provides the formation of diverse carbon-sulfur bonds via a highly efficient decarbonylative process.

Anti-Markovnikov stereoselective hydroamination and hydrothiolation of (hetero)aromatic alkynes using a metal-free cyclic trimeric phosphazene base

Hydroamination and hydrothiolation are the most efficient and completely atom-economical process to construct important enamine and vinyl sulfide intermediates in pharmaceutical and organic chemistry. The cyclic trimeric phosphazene base (CTPB) showed gre