1-Chloro-4-{[(methylsulfanyl)methyl]sulfanyl}benzene

Base Information

Chemical Name:1-Chloro-4-{[(methylsulfanyl)methyl]sulfanyl}benzene
CAS No.:62926-92-5
Molecular Formula:C8H9ClS2
Molecular Weight:204.744
Hs Code.:
DSSTox Substance ID:DTXSID90490577
Wikidata:Q82334418

Synonyms:62926-92-5;1-Chloro-4-{[(methylsulfanyl)methyl]sulfanyl}benzene;DTXSID90490577

Suppliers and Price of 1-Chloro-4-{[(methylsulfanyl)methyl]sulfanyl}benzene

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1-Chloro-4-{[(methylsulfanyl)methyl]sulfanyl}benzene

Chemical Property:

XLogP3:3.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:203.9834203
Heavy Atom Count:11
Complexity:100

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CSCSC1=CC=C(C=C1)Cl

Technology Process of 1-Chloro-4-{[(methylsulfanyl)methyl]sulfanyl}benzene

There total 2 articles about 1-Chloro-4-{[(methylsulfanyl)methyl]sulfanyl}benzene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 93.0%

: 2949-92-0,31761-75-8
methanethiosulfonic acid S-methyl ester

: 593-71-5
Chloroiodomethane

: 106-54-7
p-Chlorothiophenol

: 62926-92-5
1-chloro-4-{[(methylsulfanyl)methyl]sulfanyl}benzene

Guidance literature:: methanethiosulfonic acid S-methyl ester; Chloroiodomethane; In tetrahydrofuran; at -78 ℃; for 0.0833333h; Inert atmosphere;

With methyllithium lithium bromide; In tetrahydrofuran; diethyl ether; for 1h; Inert atmosphere;

p-Chlorothiophenol; With sodium iodide; In tetrahydrofuran; diethyl ether; N,N-dimethyl-formamide; at 0 - 20 ℃; for 6h; chemoselective reaction; Inert atmosphere;
DOI:10.1039/d0cc04896h