Phenol, 2-[1-(1H-imidazol-1-yl)-2-(propylthio)ethenyl]-, (Z)-

Base Information

Chemical Name:Phenol, 2-[1-(1H-imidazol-1-yl)-2-(propylthio)ethenyl]-, (Z)-
CAS No.:111809-00-8
Molecular Formula:C₁₄H₁₆N₂OS
Molecular Weight:260.36
Hs Code.:
DSSTox Substance ID:DTXSID201182449
Mol file:111809-00-8.mol

Synonyms:DTXSID201182449;Phenol, 2-[1-(1H-imidazol-1-yl)-2-(propylthio)ethenyl]-, (Z)-;111809-00-8

Suppliers and Price of Phenol, 2-[1-(1H-imidazol-1-yl)-2-(propylthio)ethenyl]-, (Z)-

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 Phenol, 2-[1-(1H-imidazol-1-yl)-2-(propylthio)ethenyl]-, (Z)-

Chemical Property:

XLogP3:2.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:260.09833431
Heavy Atom Count:18
Complexity:283

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCSC=C(C1=CC=CC=C1O)N2C=CN=C2
Isomeric SMILES:CCCS/C=C(/C1=CC=CC=C1O)\N2C=CN=C2

Technology Process of Phenol, 2-[1-(1H-imidazol-1-yl)-2-(propylthio)ethenyl]-, (Z)-

There total 1 articles about Phenol, 2-[1-(1H-imidazol-1-yl)-2-(propylthio)ethenyl]-, (Z)- 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:

: 288-32-4
1H-imidazole

: 111809-48-4
2-n-propylthio-2'-hydroxyacetophenone

: 111788-93-3
2-((E)-1-Imidazol-1-yl-2-propylsulfanyl-vinyl)-phenol

: 111809-00-8
2-((Z)-1-Imidazol-1-yl-2-propylsulfanyl-vinyl)-phenol

Guidance literature:: With thionyl chloride; Yield given. Multistep reaction. Yields of byproduct given; 1.) CH₂Cl₂, 30 min, room temperature, 2.) CH₂Cl₂, room temperature;
DOI:10.1248/cpb.39.2301