(S)-Methyl 2-(((benzyloxy)carbonyl)amino)-4-(methylthio)butanoate

≥95%

Reagent Code: #53004
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CAS Number 56762-93-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 297.37 g/mol
Formula C₁₄H₁₉NO₄S
badge Registry Numbers
MDL Number MFCD00145551
thermostat Physical Properties
Melting Point 41-43°C
Boiling Point 453.622°C at 760 mmHg
inventory_2 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)

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿880.00
inventory 250mg
10-20 days ฿280.00
inventory 5g
10-20 days ฿2,140.00
(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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