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L-Leucine, 4-nitrophenyl ester, monohydrochloride

Base Information
  • Chemical Name:L-Leucine, 4-nitrophenyl ester, monohydrochloride
  • CAS No.:75691-76-8
  • Molecular Formula:C12H16N2O4.ClH
  • Molecular Weight:288.72700
  • Hs Code.:
L-Leucine, 4-nitrophenyl ester, monohydrochloride

Synonyms:(S)-2-Amino-4-methyl-pentanoic acid 4-nitro-phenyl ester;hydrochloride;

Suppliers and Price of L-Leucine, 4-nitrophenyl ester, monohydrochloride
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
  • TRC
  • H-Leu-onphydrochloride
  • 1g
  • $ 75.00
  • TRC
  • H-Leu-onphydrochloride
  • 500mg
  • $ 65.00
  • TRC
  • H-Leu-onphydrochloride
  • 250mg
  • $ 55.00
  • TRC
  • H-Leu-onphydrochloride
  • 100mg
  • $ 45.00
Total 2 raw suppliers
Chemical Property of L-Leucine, 4-nitrophenyl ester, monohydrochloride
Chemical Property:
  • PSA:98.14000 
  • LogP:3.89910 
Purity/Quality:

≥ 98% (HPLC) *data from raw suppliers

H-Leu-onphydrochloride *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses H-Leu-onp hcl
Technology Process of L-Leucine, 4-nitrophenyl ester, monohydrochloride

There total 4 articles about L-Leucine, 4-nitrophenyl ester, monohydrochloride 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 hydrogenchloride; In diethyl ether; for 0.25h;
DOI:10.1021/ja00411a009
Guidance literature:
Multi-step reaction with 2 steps
1: 1.) sulfuric acid, 2.) dicyclohexylcarbodiimide / 1.) ethyl acetate, 2.) -10 deg C, 2 h; room temperature
2: 59 percent / hydrogen chloride gas / diethyl ether / 0.25 h
With hydrogenchloride; sulfuric acid; dicyclohexyl-carbodiimide; In diethyl ether;
DOI:10.1021/ja00411a009
Guidance literature:
Multi-step reaction with 2 steps
1: 1.) sulfuric acid, 2.) dicyclohexylcarbodiimide / 1.) ethyl acetate, 2.) -10 deg C, 2 h; room temperature
2: 59 percent / hydrogen chloride gas / diethyl ether / 0.25 h
With hydrogenchloride; sulfuric acid; dicyclohexyl-carbodiimide; In diethyl ether;
DOI:10.1021/ja00411a009
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