R-1-Boc-3-pyrrolidinecarboxylic acid

97%

Reagent Code: #229841
label
Alias (R)-1-Boc-3-carboxypyrrolidine
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CAS Number 72925-16-7

science Other reagents with same CAS 72925-16-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.25 g/mol
Formula C₁₀H₁₇NO₄
badge Registry Numbers
MDL Number MFCD03094727
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its protected amine group and carboxylic acid functionality make it ideal for peptide coupling and heterocycle formation. Commonly employed in the preparation of drug candidates targeting central nervous system disorders, cardiovascular diseases, and metabolic conditions. The Boc-protected pyrrolidine scaffold is valued for enhancing metabolic stability and influencing pharmacokinetic properties in final drug molecules.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿410.00
1g
10-20 days ฿970.00
5g
10-20 days ฿2,370.00
25g
10-20 days ฿10,870.00
100g
10-20 days ฿40,350.00
R-1-Boc-3-pyrrolidinecarboxylic acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its protected amine group and carboxylic acid functionality make it ideal for peptide coupling and heterocycle formation. Commonly employed in the preparation of drug candidates targeting central nervous system disorders, cardiovascular diseases, and metabolic conditions. The Boc-protected pyrrolidine scaffold is valued for enha

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its protected amine group and carboxylic acid functionality make it ideal for peptide coupling and heterocycle formation. Commonly employed in the preparation of drug candidates targeting central nervous system disorders, cardiovascular diseases, and metabolic conditions. The Boc-protected pyrrolidine scaffold is valued for enhancing metabolic stability and influencing pharmacokinetic properties in final drug molecules.

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