L-Proline methyl ester hydrochloride
98%
Reagent
Code: #105344
Alias
L-Proline methyl ester hydrochloride
CAS Number
2133-40-6
blur_circular Chemical Specifications
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Molecular Information
Weight
165.62 g/mol
Formula
C₆H₁₂ClNO₂
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Registry Numbers
EC Number
218-363-0
MDL Number
MFCD00012708
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Physical Properties
Melting Point
69-71 °C(lit.)
Boiling Point
55 °C / 11mmHg
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Storage & Handling
Storage
Room temperature, dry, sealed
description Product Description
L-Proline methyl ester hydrochloride is widely used in organic synthesis, particularly in peptide chemistry. It serves as a building block for the preparation of proline-containing peptides and peptidomimetics, which are essential in drug discovery and development. The compound is also employed in asymmetric synthesis, where it acts as a chiral auxiliary to induce stereoselectivity in reactions, leading to the production of enantiomerically pure compounds. Additionally, it finds application in the synthesis of biologically active molecules, including inhibitors and ligands for various enzymes and receptors. Its stability and reactivity make it a valuable reagent in medicinal chemistry and biochemical research.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | White Powder |
Purity (%) | 97.5-100 |
Melting Point | 70-80 |
Specific Rotation [α]20/D (C=1, H2O) | -33 to -30 |
Infrared Spectrometry | Conforms To Structure |
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L-Proline methyl ester hydrochloride
L-Proline methyl ester hydrochloride is widely used in organic synthesis, particularly in peptide chemistry. It serves as a building block for the preparation of proline-containing peptides and peptidomimetics, which are essential in drug discovery and development. The compound is also employed in asymmetric synthesis, where it acts as a chiral auxiliary to induce stereoselectivity in reactions, leading to the production of enantiomerically pure compounds. Additionally, it finds application in the synthesis of biologically active molecules, including inhibitors and ligands for various enzymes and receptors. Its stability and reactivity make it a valuable reagent in medicinal chemistry and biochemical research.
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