41383-84-0

Basic information

• Product Name: [2-(sulfanylmethyl)phenyl]methanethiol
• Synonyms: [2-(sulfanylmethyl)phenyl]methanethiol
• CAS NO: 41383-84-0
• Molecular Formula: C₈H₁₀S₂
• Molecular Weight: 170.295000
• Mol File: 41383-84-0.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 284.3 °C at 760 mmHg
• Flash Point: 115.1 °C
• Appearance: /
• Density: 1.134 g/cm³
• PKA: 9.25±0.10(Predicted)
• CAS DataBase Reference: [2-(sulfanylmethyl)phenyl]methanethiol(CAS DataBase Reference)
• NIST Chemistry Reference: [2-(sulfanylmethyl)phenyl]methanethiol(41383-84-0)
• EPA Substance Registry System: [2-(sulfanylmethyl)phenyl]methanethiol(41383-84-0)

Safety Data

• Hazardous Substances Data: 41383-84-0(Hazardous Substances Data)

Usage

General Description

[2-(sulfanylmethyl)phenyl]methanethiol is a chemical compound with a molecular formula C8H10S2. It is a thiol derivative with a phenyl group and a methanethiol group attached to a sulfur atom. [2-(sulfanylmethyl)phenyl]methanethiol is commonly used in organic synthesis and chemical research as a building block for more complex molecules. It has a distinct smell and is known to be highly reactive due to the presence of the thiol group, which makes it useful in various chemical processes. Additionally, it can also be used as a chemical intermediate in the production of pharmaceuticals, agricultural chemicals, and other products.

InChI:InChI=1/C8H10S2/c9-5-7-3-1-2-4-8(7)6-10/h1-4,9-10H,5-6H2

Upstream product

• 91-13-4 α,α'-dibromo-o-xylene 
• 16464-64-5 benzene-1,2-bismethaneisothiouronium dibromide 
• 612-12-4 o-Xylylene dichloride 

Downstream Products

• 3886-39-3 1,4-dihydrobenzo-2,3-dithiane 
• 29906-21-6 2-phenyl-1,3-dithia-5,6-benzcycloheptene 
• 54738-38-4 2-[4-(1,5-dihydro-benzo[e][1,3]dithiepin-3-yl)-styryl]-5-nitro-1-vinyl-1H-imidazole 
• 24293-19-4 1,2-Bis<(methylthio)methyl>benzene 
• 442519-01-9 α,α'-bis(3-hydroxy-3-methyl-1-thiabutyl)-o-xylene 
• 688310-93-2 1,2-bis(4-(3,3-dimethyl-2,4-dioxacyclohexanyl)-2-thiapentyl)benzene 
• 81098-00-2 Ni((P(C₆H₅)2)2C₂H₄)((SCH₂)2C₆H₄) 
• 930093-50-8 (PNP(Ph))Ni(o-SCH₂C₆H₄CH₂S) 
• 189184-22-3 CpTi(OC₆H₃-2,6-i-Pr₂)((SCH₂)₂C₆H₄) 

Relevant articles and documents

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Thioacetate deprotection

A method of thioacetate deprotection by providing a compound of the formula R1—S—CO—R2, and reacting the compound with a quaternary ammonium cyanide salt in the presence of a protic solvent in an inert atmosphere to convert the compound to a product of the formula R1—SH. R1 is an organic group in which the bonding to sulfur is through a saturated carbon, and R2 is an aliphatic group.

Stereoselective reductase-catalysed deoxygenation of sulfoxides in aerobic and anaerobic bacteria.

Direct and indirect evidence, of unexpected stereoselective reductase-catalysed deoxygenations of sulfoxides, was found. The deoxygenations proceeded simultaneously, with the expected dioxygenase-catalysed asymmetric sulfoxidation of sulfides, during some biotransformations with the aerobic bacterium Pseudomonas putida UV4. Stereoselective reductase-catalysed asymmetric deoxygenation of racemic alkylaryl, dialkyl and phenolic sulfoxides was observed, without evidence of the reverse sulfoxidation reaction, using anaerobic bacterial strains. A purified dimethyl sulfoxide reductase, obtained from the intact cells of the anaerobic bacterium Citrobacter braakii DMSO 11, yielded, from the corresponding racemates, enantiopure alkylaryl sulfoxide and thiosulfinate samples.