(S)-Methyl 2-(((benzyloxy)carbonyl)amino)-4-(methylthio)butanoate
≥95%
Reagent
Code: #53004
CAS Number
56762-93-7
blur_circular Chemical Specifications
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Molecular Information
Weight
297.37 g/mol
Formula
C₁₄H₁₉NO₄S
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Registry Numbers
MDL Number
MFCD00145551
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Physical Properties
Melting Point
41-43°C
Boiling Point
453.622°C at 760 mmHg
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Storage & Handling
Storage
Room temperature, dry and sealed
description Product Description
This compound is primarily utilized in the synthesis of peptides and other biologically active molecules. It serves as a key intermediate in the production of cysteine derivatives, which are essential in the development of pharmaceuticals targeting various diseases. Its structure allows for selective modifications, making it valuable in the design of enzyme inhibitors and receptor modulators. Additionally, it is employed in research settings to study the role of sulfur-containing amino acids in protein folding and stability. The compound’s protective groups enable controlled reactions, facilitating its use in complex organic synthesis processes.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | White to yellow solid |
Purity | 94.5-100 |
Infrared Spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Note | This product is a low melting point solid and may change state in different environments (solid, liquid, or semi-solid) |
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(S)-Methyl 2-(((benzyloxy)carbonyl)amino)-4-(methylthio)butanoate
This compound is primarily utilized in the synthesis of peptides and other biologically active molecules. It serves as a key intermediate in the production of cysteine derivatives, which are essential in the development of pharmaceuticals targeting various diseases. Its structure allows for selective modifications, making it valuable in the design of enzyme inhibitors and receptor modulators. Additionally, it is employed in research settings to study the role of sulfur-containing amino acids in protein folding and stability. The compound’s protective groups enable controlled reactions, facilitating its use in complex organic synthesis processes.
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