L-Proline methyl ester hydrochloride

98%

Reagent Code: #105344
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Alias L-Proline methyl ester hydrochloride
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CAS Number 2133-40-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 165.62 g/mol
Formula C₆H₁₂ClNO₂
badge Registry Numbers
EC Number 218-363-0
MDL Number MFCD00012708
thermostat Physical Properties
Melting Point 69-71 °C(lit.)
Boiling Point 55 °C / 11mmHg
inventory_2 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

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days $24.07
inventory 1g
10-20 days $15.47
inventory 25g
10-20 days $34.38
inventory 100g
10-20 days $108.30
inventory 500g
10-20 days $527.76
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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