L-Prolinamide hydrochloride

98%

Reagent Code: #62979
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CAS Number 42429-27-6

science Other reagents with same CAS 42429-27-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 150.61 g/mol
Formula C₅H₁₀N₂OHC
badge Registry Numbers
MDL Number MFCD00058156
thermostat Physical Properties
Melting Point 178 °C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

L-Prolinamide hydrochloride is widely used in organic synthesis as a chiral building block for the preparation of various pharmaceuticals and bioactive compounds. It serves as a key intermediate in the synthesis of peptide-based drugs, enabling the introduction of proline derivatives into peptide chains to enhance stability and biological activity. Additionally, it is employed in asymmetric catalysis, particularly in the development of chiral catalysts for enantioselective reactions, which are crucial in producing optically pure compounds. Its application extends to the field of medicinal chemistry, where it is utilized in the design of enzyme inhibitors and receptor ligands, contributing to drug discovery and development.

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Test Parameter Specification
APPEARANCE White to Light Yellow Solid
Purity (%) 97.5-100
Solubility (Color) Colorless to Light Yellow
Solubility (Turbidity) 50 mg/mL, H2O, Clear
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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inventory 1g
10-20 days ฿549.00

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L-Prolinamide hydrochloride
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L-Prolinamide hydrochloride is widely used in organic synthesis as a chiral building block for the preparation of various pharmaceuticals and bioactive compounds. It serves as a key intermediate in the synthesis of peptide-based drugs, enabling the introduction of proline derivatives into peptide chains to enhance stability and biological activity. Additionally, it is employed in asymmetric catalysis, particularly in the development of chiral catalysts for enantioselective reactions, which are crucial in

L-Prolinamide hydrochloride is widely used in organic synthesis as a chiral building block for the preparation of various pharmaceuticals and bioactive compounds. It serves as a key intermediate in the synthesis of peptide-based drugs, enabling the introduction of proline derivatives into peptide chains to enhance stability and biological activity. Additionally, it is employed in asymmetric catalysis, particularly in the development of chiral catalysts for enantioselective reactions, which are crucial in producing optically pure compounds. Its application extends to the field of medicinal chemistry, where it is utilized in the design of enzyme inhibitors and receptor ligands, contributing to drug discovery and development.

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