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1-Phenylethyl chloroacetate

Base Information
  • Chemical Name:1-Phenylethyl chloroacetate
  • CAS No.:72939-47-0
  • Deprecated CAS:115729-62-9
  • Molecular Formula:C10H11ClO2
  • Molecular Weight:198.649
  • Hs Code.:
  • NSC Number:404452,46001
  • DSSTox Substance ID:DTXSID00888325
  • Nikkaji Number:J447.275F
  • Mol file:72939-47-0.mol
1-Phenylethyl chloroacetate

Synonyms:1-Phenylethyl chloroacetate;72939-47-0;Acetic acid, chloro-, 1-phenylethyl ester;Acetic acid, 2-chloro-, 1-phenylethyl ester;Acetic acid, 1-phenylethyl ester;SCHEMBL1766149;DTXSID00888325;NSC46001;NSC 46001;NSC-46001;NSC404452;NSC 404452;NSC-404452;2-Chloroacetic acid 1-phenylethyl ester

Suppliers and Price of 1-Phenylethyl chloroacetate
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 5 raw suppliers
Chemical Property of 1-Phenylethyl chloroacetate
Chemical Property:
  • Vapor Pressure:0.0145mmHg at 25°C 
  • Boiling Point:257.5°C at 760 mmHg 
  • Flash Point:117.6°C 
  • PSA:26.30000 
  • Density:1.162g/cm3 
  • LogP:2.52960 
  • XLogP3:2.6
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:4
  • Exact Mass:198.0447573
  • Heavy Atom Count:13
  • Complexity:164
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C1=CC=CC=C1)OC(=O)CCl
Technology Process of 1-Phenylethyl chloroacetate

There total 3 articles about 1-Phenylethyl chloroacetate 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:
Guidance literature:
With triethylamine; In diethyl ether; for 1h; Ambient temperature;
DOI:10.1021/jm00119a015
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