Newblue CHEM-- Meth...

Newblue CHEM--	Methoxycarbonyl-L-tert-leucine_

Newblue CHEM-- Methoxycarbonyl-L-tert-leucine_

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162537-11-3 Methoxycarbonyl-L-tert-leucine Methoxycarbonyl-L-tert-leucine

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Details:

 
Product Name: Methoxycarbonyl-L-tert-leucine
Synonyms: MOC-L-tert.Leucine;MOC-L-tert. Leucin;(S)-2-Methoxycarbonylamino-3,3-dimethylbutyric acid;Methoxycarbonyl-L-tert-leucine;N-(Methoxycarbonyl)-3-methyl-L-valine;L-Valine,N-(Methoxycarbonyl)-3-Methyl-;(S)-2-(MethoxycarbonylaMino)-3,3-diMethylbutanoic acid;Moc-L-tert-lecine
CAS: 162537-11-3
MF: C8H15NO4
MW: 189.21
EINECS:
Product Categories: Amino Acid Derivatives;Amino Acids 13C, 2H, 15N;Amino Acids & Derivatives;Chiral Reagents
Mol File: 162537-11-3.mol
Methoxycarbonyl-L-tert-leucine Structure
Methoxycarbonyl-L-tert-leucine Chemical Properties
Melting point 1090C
solubility Soluble in ethyl acetate and methanol.
InChIKey NWPRXAIYBULIEI-RXMQYKEDSA-N
Safety Information
MSDS Information
Methoxycarbonyl-L-tert-leucine Usage And Synthesis
Description Methoxycarbonyl-L-tert-leucine is a kind of amino acid deriviative. It is a very useful intermediate for efficient synthesis of the HIV protease inhibitor BMS-232632 as well as atazanavir bisulfate. 
References Zhongmin Xu, †, et al. "Process Research and Development for an Efficient Synthesis of the HIV Protease Inhibitor BMS-232632." Organic Process Research & Development 6.3(2002):323-328.
Simhadri, Srinivas. "Process for the preparation of atazanavir bisulfate." (2016).
# q=14328-63-3
Chemical Properties White Solid

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