Allyl benzyl ethanol

Base Information

Chemical Name:Allyl benzyl ethanol
CAS No.:39615-80-0
Molecular Formula:C12H16O
Molecular Weight:176.258
Hs Code.:
DSSTox Substance ID:DTXSID201283922

Synonyms:Allyl benzyl ethanol;39615-80-0;2-benzylpent-4-en-2-ol;SCHEMBL8483770;WMWPOGZEGNDCAQ-UHFFFAOYSA-N;DTXSID201283922;AKOS018291794;alpha-Methyl-alpha-2-propen-1-ylbenzeneethanol

Suppliers and Price of Allyl benzyl ethanol

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 0 raw suppliers

Chemical Property of Allyl benzyl ethanol

Chemical Property:

XLogP3:2.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:4
Exact Mass:176.120115130
Heavy Atom Count:13
Complexity:159

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(CC=C)(CC1=CC=CC=C1)O

Technology Process of Allyl benzyl ethanol

There total 11 articles about Allyl benzyl ethanol 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: 60.0%

: 141-82-2
malonic acid

: 7393-43-3
tetraallyl tin

: 103-79-7,136675-26-8
1-phenyl-acetone

: 39615-80-0
d,l-1-phenyl-2-methyl-4-penten-2-ol

Guidance literature:: In neat (no solvent); addn. of ketone to organotin compd., ratio of educts: aldehyd:tin compd.=1:1, stirred, 24h, 95°C, acidolysis by addn. of stoich. amt of malonic acid in anhydrous ether, 48h, reflux, pptn. of malonate by addn.of pentane; alcohol detected by NMR, IR and chromy.;
DOI:10.1016/S0022-328X(00)82877-6