1-Buten-1-one, 2-phenyl-

Base Information

Chemical Name:1-Buten-1-one, 2-phenyl-
CAS No.:20452-67-9
Molecular Formula:C10H10 O
Molecular Weight:146.189
Hs Code.:2914399090
Mol file:20452-67-9.mol

Synonyms:Ketene,ethylphenyl- (7CI,8CI); 2-Phenyl-1-buten-1-one; Ethylphenylketene;Phenylethylketene

Suppliers and Price of 1-Buten-1-one, 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 3 raw suppliers

Chemical Property of 1-Buten-1-one, 2-phenyl-

Chemical Property:

Boiling Point:198.1°Cat760mmHg
Flash Point:69.3°C
PSA：17.07000
Density:0.957g/cm³
LogP:2.31160

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 1-Buten-1-one, 2-phenyl-

There total 4 articles about 1-Buten-1-one, 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:

: 1519-21-7
2-phenylbutyric anhydride

: 20452-67-9
phenylethylketene

: 90-27-7
2-Phenylbutyric acid

Guidance literature:: at -33.15 ℃; Further Variations:; Temperatures; Product distribution; reduced pressure distillation;
DOI:10.1002/1522-2675(20010613)84:6<1405::AID-HLCA1405>3.0.CO;2-G

Reference yield:

: 90-27-7
2-Phenylbutyric acid

: 20452-67-9
phenylethylketene

Guidance literature:: Multi-step reaction with 2 steps

1: SOCl₂

2: 48 percent / Et₃N / tetrahydrofuran / 3 h / Ambient temperature

With thionyl chloride; triethylamine; In tetrahydrofuran;
DOI:10.1021/ja00305a012