4-(Butylsulfanyl)phenol

Base Information

Chemical Name:4-(Butylsulfanyl)phenol
CAS No.:1077-25-4
Molecular Formula:C10H14OS
Molecular Weight:182.287
Hs Code.:
DSSTox Substance ID:DTXSID701315794
Nikkaji Number:J2.096.729C
Mol file:1077-25-4.mol

Synonyms:4-(butylsulfanyl)phenol;1077-25-4;4-butylsulfanylphenol;4-(Butylthio)phenol;SCHEMBL4399477;DTXSID701315794

Suppliers and Price of 4-(Butylsulfanyl)phenol

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-(Butylsulfanyl)phenol

Chemical Property:

XLogP3:3.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:182.07653624
Heavy Atom Count:12
Complexity:108

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCSC1=CC=C(C=C1)O

Technology Process of 4-(Butylsulfanyl)phenol

There total 10 articles about 4-(Butylsulfanyl)phenol 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: 73.0%

: 629-45-8
dibutyl disulfide

: 540-38-5
p-Iodophenol

: 1077-25-4
4-hydroxyphenylbutylsulfide

Guidance literature:: With [2,2]bipyridinyl; nickel dibromide; zinc; In N,N-dimethyl-formamide; at 110 ℃; for 48h;
DOI:10.1021/jo040184q

Reference yield:

: 156-43-4
4-Ethoxyaniline

: 1077-25-4
4-hydroxyphenylbutylsulfide

Guidance literature:: With hydrogenchloride; at 70 - 90 ℃; Diazotization_.Erwaermen des entstandenen 4-Aethoxy-1-butylmercapto-benzols mit wss. HBr und Essigsaeure auf 75-85grad und Kochen des erhaltenen Oels mit wss.-aethanol. NaOH;
DOI:10.1021/ja01330a061