(2S,4S)-1-Boc-4-Aminopyrrolidine-2-carboxylic acid

97%

Reagent Code: #234961
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CAS Number 132622-66-3

science Other reagents with same CAS 132622-66-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.26 g/mol
Formula C₁₀H₁₈N₂O₄
badge Registry Numbers
MDL Number MFCD03427029
thermostat Physical Properties
Melting Point >266°C
Boiling Point 371.1°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Widely used in pharmaceutical synthesis, this compound serves as a chiral building block for the preparation of bioactive molecules, particularly protease inhibitors and antiviral agents. Its protected amine and carboxylic acid functionalities allow selective coupling in peptide-like structures, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. The stereochemistry supports high selectivity in asymmetric synthesis, enhancing drug potency and reducing side effects. Commonly employed in solid-phase and solution-phase synthesis of drug candidates targeting neurological disorders and metabolic diseases.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿770.00
inventory 1g
10-20 days ฿2,610.00
inventory 10g
10-20 days ฿22,690.00
inventory 5g
10-20 days ฿11,360.00
(2S,4S)-1-Boc-4-Aminopyrrolidine-2-carboxylic acid
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Widely used in pharmaceutical synthesis, this compound serves as a chiral building block for the preparation of bioactive molecules, particularly protease inhibitors and antiviral agents. Its protected amine and carboxylic acid functionalities allow selective coupling in peptide-like structures, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. The stereochemistry supports high selectivity in asymmetric synthesis, enhancing drug potency and reducing side effects. Co

Widely used in pharmaceutical synthesis, this compound serves as a chiral building block for the preparation of bioactive molecules, particularly protease inhibitors and antiviral agents. Its protected amine and carboxylic acid functionalities allow selective coupling in peptide-like structures, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. The stereochemistry supports high selectivity in asymmetric synthesis, enhancing drug potency and reducing side effects. Commonly employed in solid-phase and solution-phase synthesis of drug candidates targeting neurological disorders and metabolic diseases.

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