3-Buten-1-ol, 2-phenyl-

Base Information

Chemical Name:3-Buten-1-ol, 2-phenyl-
CAS No.:6052-63-7
Molecular Formula:C10H12O
Molecular Weight:148.205
Hs Code.:2906299090
DSSTox Substance ID:DTXSID70290613
Nikkaji Number:J121.199D
Mol file:6052-63-7.mol

Synonyms:3-Buten-1-ol, 2-phenyl-;6052-63-7;Benzeneethanol, .beta.-ethenyl-;2-Phenyl-3-buten-1-ol;2-Phenyl-3-buten-1-ol #;SCHEMBL4667833;DTXSID70290613;Phenethyl alcohol, .beta.-vinyl-

Suppliers and Price of 3-Buten-1-ol, 2-phenyl-

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 4 raw suppliers

Chemical Property of 3-Buten-1-ol, 2-phenyl-

Chemical Property:

Boiling Point:240.2±9.0 °C(Predicted)
PKA:14.56±0.10(Predicted)
PSA：20.23000
Density:0.997±0.06 g/cm3(Predicted)
LogP:1.94850
XLogP3:2.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:148.088815002
Heavy Atom Count:11
Complexity:114

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

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

Technology Process of 3-Buten-1-ol, 2-phenyl-

There total 35 articles about 3-Buten-1-ol, 2-phenyl- 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: 97.0%

: 50-00-0,30525-89-4,61233-19-0
formaldehyd

: 4392-24-9
3-bromo-1-phenyl-1-propenyl bromide

: 6052-63-7
2-phenylbut-3-en-1-ol

Guidance literature:: With tin(II) chloride dihdyrate; potassium iodide; In acetone; at 20 ℃; chemoselective reaction;
DOI:10.1055/s-0030-1260757