(S)-Isopropyl 2-amino-3-hydroxypropanoate hydrochloride

97%

Reagent Code: #87179
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CAS Number 37592-53-3

science Other reagents with same CAS 37592-53-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 183.63 g/mol
Formula C₆H₁₄ClNO₃
badge Registry Numbers
MDL Number MFCD31630717
inventory_2 Storage & Handling
Storage room temperature, inert gas storage

description Product Description

This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the production of chiral drugs. Its role as a chiral building block is crucial in the development of enantiomerically pure medications, which are often more effective and have fewer side effects. Additionally, it finds application in the preparation of amino acid derivatives, which are essential in peptide synthesis and drug design. Its hydrochloride form enhances solubility, making it suitable for use in various aqueous-based reactions and formulations.

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Test Parameter Specification
Appearance Solid
Purity (%) 96.5-100
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿495.00
inventory 1g
10-20 days ฿1,251.00
inventory 5g
10-20 days ฿4,392.00

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(S)-Isopropyl 2-amino-3-hydroxypropanoate hydrochloride
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This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the production of chiral drugs. Its role as a chiral building block is crucial in the development of enantiomerically pure medications, which are often more effective and have fewer side effects. Additionally, it finds application in the preparation of amino acid derivatives, which are essential in peptide synthesis and drug design. Its hydrochloride form enhances solubility, making it suitable for use in various aqu

This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the production of chiral drugs. Its role as a chiral building block is crucial in the development of enantiomerically pure medications, which are often more effective and have fewer side effects. Additionally, it finds application in the preparation of amino acid derivatives, which are essential in peptide synthesis and drug design. Its hydrochloride form enhances solubility, making it suitable for use in various aqueous-based reactions and formulations.

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