D-Proline methyl ester hydrochloride

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Reagent Code: #67181
label
Alias D-proline methyl ester hydrochloride
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CAS Number 65365-28-8

science Other reagents with same CAS 65365-28-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 165.62 g/mol
Formula C₆H₁₁NO₂HCl
badge Registry Numbers
MDL Number MFCD00083685
thermostat Physical Properties
Melting Point 69-71°C
inventory_2 Storage & Handling
Storage -20°C, sealed

description Product Description

Used in organic synthesis as a chiral building block for the preparation of pharmaceuticals and bioactive compounds. It serves as a key intermediate in the synthesis of peptides and peptidomimetics, enabling the introduction of proline derivatives into complex molecules. Its chiral nature makes it valuable in asymmetric synthesis, particularly in the development of enantioselective catalysts and ligands. Additionally, it is employed in the study of enzyme mechanisms and protein folding due to its ability to mimic natural amino acids.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (Non-Aqueous Titration) 96.5-103.5%
Specific Rotation (α20/D c=1, water) 31-35
Melting point 71-75
APPEARANCE WHITE TO LIGHT YELLOW POWDER
Infrared Spectrometry Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿700.00
inventory 250mg
10-20 days ฿290.00
inventory 25g
10-20 days ฿2,680.00
inventory 1g
10-20 days ฿410.00

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D-Proline methyl ester hydrochloride
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Used in organic synthesis as a chiral building block for the preparation of pharmaceuticals and bioactive compounds. It serves as a key intermediate in the synthesis of peptides and peptidomimetics, enabling the introduction of proline derivatives into complex molecules. Its chiral nature makes it valuable in asymmetric synthesis, particularly in the development of enantioselective catalysts and ligands. Additionally, it is employed in the study of enzyme mechanisms and protein folding due to its ability

Used in organic synthesis as a chiral building block for the preparation of pharmaceuticals and bioactive compounds. It serves as a key intermediate in the synthesis of peptides and peptidomimetics, enabling the introduction of proline derivatives into complex molecules. Its chiral nature makes it valuable in asymmetric synthesis, particularly in the development of enantioselective catalysts and ligands. Additionally, it is employed in the study of enzyme mechanisms and protein folding due to its ability to mimic natural amino acids.

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