CID 54279058

Base Information

Chemical Name:CID 54279058
CAS No.:117721-77-4
Molecular Formula:C13H18O
Molecular Weight:190.285
Hs Code.:
DSSTox Substance ID:DTXSID90710267

Synonyms:3-(4-tert-butylphenyl)prop-2-en-1-ol;DTXSID90710267;AKOS017888547

Suppliers and Price of CID 54279058

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 CID 54279058

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:190.135765193
Heavy Atom Count:14
Complexity:180

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)C1=CC=C(C=C1)C=CCO

Technology Process of CID 54279058

There total 11 articles about CID 54279058 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: 96.0%

: 158010-17-4
ethyl (E)-3-[4-(tert-butylphenyl)]-2-propenoate

: 117721-77-4
(E)-3-(4-(tert-butyl)phenyl)prop-2-en-1-ol

Guidance literature:: With diisobutylaluminium hydride; In hexane; dichloromethane; 1.) 15 min, - 78 deg C; 2.) 16 h, room temp.;
DOI:10.1016/S0040-4020(01)89368-6

Reference yield: 82.0%

: 27798-45-4
1-allyl-4-(tert-butyl)benzene

: 117721-77-4
(E)-3-(4-(tert-butyl)phenyl)prop-2-en-1-ol

Guidance literature:: With hydrogenchloride; water; oxygen; palladium dichloride; In dimethyl sulfoxide; at 100 ℃; for 24h; under 760.051 Torr; regioselective reaction; Green chemistry;
DOI:10.1002/adsc.201701324