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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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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