4-(Ethylsulfanyl)-3-methylphenol

Base Information

Chemical Name:4-(Ethylsulfanyl)-3-methylphenol
CAS No.:67126-92-5
Molecular Formula:C9H12OS
Molecular Weight:168.26
Hs Code.:
DSSTox Substance ID:DTXSID10708181
Wikidata:Q82642334

Synonyms:67126-92-5;4-(Ethylsulfanyl)-3-methylphenol;SCHEMBL11731334;DTXSID10708181

Suppliers and Price of 4-(Ethylsulfanyl)-3-methylphenol

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 1 raw suppliers

Chemical Property of 4-(Ethylsulfanyl)-3-methylphenol

Chemical Property:

XLogP3:2.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:168.06088618
Heavy Atom Count:11
Complexity:116

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCSC1=C(C=C(C=C1)O)C

Technology Process of 4-(Ethylsulfanyl)-3-methylphenol

There total 3 articles about 4-(Ethylsulfanyl)-3-methylphenol 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:

: 2-ethylsulfanyl-5-methoxy-toluene

: 67126-92-5
4-ethylsulfanyl-3-methyl-phenol

Guidance literature:: With hydrogen bromide; acetic acid; at 120 - 130 ℃;
DOI:10.1021/ja01326a079

Reference yield:

: 698-81-7
5-methoxy-2-mercapto-toluene

: 67126-92-5
4-ethylsulfanyl-3-methyl-phenol

Guidance literature:: Multi-step reaction with 2 steps

1: aqueous NaOH

2: glacial acetic acid; aqueous HBr / 120 - 130 °C

With sodium hydroxide; hydrogen bromide; acetic acid;
DOI:10.1021/ja01326a079