L-Valine benzyl ester hydrochloride

99%

Reagent Code: #202241
label
Alias L-valine benzyl ester hydrochloride
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CAS Number 2462-34-2

science Other reagents with same CAS 2462-34-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.73 g/mol
Formula C₁₂H₁₇NO₂·HCl
badge Registry Numbers
MDL Number MFCD22422648
thermostat Physical Properties
Melting Point 138 °C
Boiling Point 285.5 °C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C, Inert Gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals and peptides, particularly in the development of protease inhibitors and other bioactive molecules. Its benzyl ester group acts as a protecting group for the carboxylic acid function during peptide coupling, allowing selective reaction at the amino group. The hydrochloride salt enhances stability and solubility in polar solvents, making it suitable for use in organic synthesis and medicinal chemistry. Commonly employed in the preparation of antibiotics, antivirals, and enzyme inhibitors where stereochemistry is critical for biological activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿840.00
inventory 100g
10-20 days ฿3,270.00
inventory 500g
10-20 days ฿14,090.00
L-Valine benzyl ester hydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals and peptides, particularly in the development of protease inhibitors and other bioactive molecules. Its benzyl ester group acts as a protecting group for the carboxylic acid function during peptide coupling, allowing selective reaction at the amino group. The hydrochloride salt enhances stability and solubility in polar solvents, making it suitable for use in organic synthesis and medicinal chemistry. Commonly employed in the preparation

Used as a chiral building block in the synthesis of pharmaceuticals and peptides, particularly in the development of protease inhibitors and other bioactive molecules. Its benzyl ester group acts as a protecting group for the carboxylic acid function during peptide coupling, allowing selective reaction at the amino group. The hydrochloride salt enhances stability and solubility in polar solvents, making it suitable for use in organic synthesis and medicinal chemistry. Commonly employed in the preparation of antibiotics, antivirals, and enzyme inhibitors where stereochemistry is critical for biological activity.

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