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VALINE BENZYL ESTER

Base Information Edit
  • Chemical Name:VALINE BENZYL ESTER
  • CAS No.:17645-51-1
  • Molecular Formula:C12H17NO2
  • Molecular Weight:207.272
  • Hs Code.:2922499990
  • Mol file:17645-51-1.mol
VALINE BENZYL ESTER

Synonyms:VALINE BENZYL ESTER;D,L-Valine Benzyl Ester;Valine Phenylmethyl Ester

Suppliers and Price of VALINE BENZYL ESTER
Supply Marketing:Edit
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
  • Usbiological
  • Valine Benzyl Ester
  • 1g
  • $ 403.00
  • Medical Isotopes, Inc.
  • ValineBenzylEster
  • 1 g
  • $ 860.00
  • ChemScene
  • Benzylvalinate
  • 1000g
  • $ 4264.00
  • American Custom Chemicals Corporation
  • VALINE BENZYL ESTER 95.00%
  • 25G
  • $ 600.00
  • American Custom Chemicals Corporation
  • VALINE BENZYL ESTER 95.00%
  • 5MG
  • $ 495.42
Total 7 raw suppliers
Chemical Property of VALINE BENZYL ESTER Edit
Chemical Property:
  • PSA:52.32000 
  • LogP:2.41340 
Purity/Quality:

97% *data from raw suppliers

Valine Benzyl Ester *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of VALINE BENZYL ESTER

There total 8 articles about VALINE BENZYL ESTER 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:
D,L-valine; With potassium carbonate; In acetone; at 40 ℃; for 0.5h;
benzyl chloride; With tetrabutylammomium bromide; In acetone; for 12h; Inert atmosphere;
Guidance literature:
With hydrogen bromide; acetic acid;
DOI:10.1021/jo50012a002
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