(S)-Alpha-allyl-proline, HCl

purum, ≥98.0% (TLC)

Reagent Code: #73178
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CAS Number 129704-91-2

science Other reagents with same CAS 129704-91-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.66 g/mol
Formula C₈H₁₃NO₂HCl
badge Registry Numbers
MDL Number MFCD06659238
thermostat Physical Properties
Melting Point 230 - 232 ℃
inventory_2 Storage & Handling
Storage room temperature

description Product Description

(S)-Alpha-allyl-proline, HCl is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key chiral building block in the development of peptide-based drugs and bioactive molecules. The compound is often employed in asymmetric synthesis to introduce specific stereochemistry into target molecules, enhancing their biological activity or selectivity. Additionally, it is used in the preparation of proline derivatives, which are essential in designing enzyme inhibitors and receptor modulators. Its application extends to medicinal chemistry, where it aids in the creation of novel therapeutic agents targeting diseases such as cancer, viral infections, and neurological disorders. The allyl group in the structure also allows for further functionalization, making it a versatile intermediate in complex chemical transformations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,070.00
inventory 250mg
10-20 days ฿26,780.00

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(S)-Alpha-allyl-proline, HCl
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(S)-Alpha-allyl-proline, HCl is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key chiral building block in the development of peptide-based drugs and bioactive molecules. The compound is often employed in asymmetric synthesis to introduce specific stereochemistry into target molecules, enhancing their biological activity or selectivity. Additionally, it is used in the preparation of proline derivatives, which are essential in designing enzyme inhibitors and receptor

(S)-Alpha-allyl-proline, HCl is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key chiral building block in the development of peptide-based drugs and bioactive molecules. The compound is often employed in asymmetric synthesis to introduce specific stereochemistry into target molecules, enhancing their biological activity or selectivity. Additionally, it is used in the preparation of proline derivatives, which are essential in designing enzyme inhibitors and receptor modulators. Its application extends to medicinal chemistry, where it aids in the creation of novel therapeutic agents targeting diseases such as cancer, viral infections, and neurological disorders. The allyl group in the structure also allows for further functionalization, making it a versatile intermediate in complex chemical transformations.

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