(3R,4R)-tert-Butyl 3-amino-4-hydroxypyrrolidine-1-carboxylate

98%

Reagent Code: #230159
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CAS Number 330681-18-0

science Other reagents with same CAS 330681-18-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.25 g/mol
Formula C₉H₁₈N₂O₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in pharmaceutical synthesis for various therapeutic areas, including diabetes treatment with DPP-4 inhibitors such as sitagliptin and vildagliptin, as well as drugs targeting neurological and psychiatric disorders. Its (3R,4R) configuration with two asymmetric centers enhances target specificity, selectivity, and metabolic stability of bioactive molecules. Commonly employed in the preparation of protease inhibitors and receptor modulators due to its favorable stereochemistry and functional group arrangement. Also utilized in medicinal chemistry for structure-activity relationship studies, enabling optimization of highly specific drug candidates against proteins or enzymes.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿390.00
inventory 250mg
10-20 days ฿1,280.00
inventory 1g
10-20 days ฿2,990.00
inventory 5g
10-20 days ฿11,960.00

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(3R,4R)-tert-Butyl 3-amino-4-hydroxypyrrolidine-1-carboxylate
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Used as a chiral building block in pharmaceutical synthesis for various therapeutic areas, including diabetes treatment with DPP-4 inhibitors such as sitagliptin and vildagliptin, as well as drugs targeting neurological and psychiatric disorders. Its (3R,4R) configuration with two asymmetric centers enhances target specificity, selectivity, and metabolic stability of bioactive molecules. Commonly employed in the preparation of protease inhibitors and receptor modulators due to its favorable stereochemist

Used as a chiral building block in pharmaceutical synthesis for various therapeutic areas, including diabetes treatment with DPP-4 inhibitors such as sitagliptin and vildagliptin, as well as drugs targeting neurological and psychiatric disorders. Its (3R,4R) configuration with two asymmetric centers enhances target specificity, selectivity, and metabolic stability of bioactive molecules. Commonly employed in the preparation of protease inhibitors and receptor modulators due to its favorable stereochemistry and functional group arrangement. Also utilized in medicinal chemistry for structure-activity relationship studies, enabling optimization of highly specific drug candidates against proteins or enzymes.

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