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

98%

Reagent Code: #231352
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CAS Number 252574-02-0

science Other reagents with same CAS 252574-02-0

blur_circular Chemical Specifications

inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of antiviral and antidiabetic drugs. Its stereochemistry allows for selective reactions in multi-step organic syntheses, making it valuable in constructing complex molecules with high enantiomeric purity. Commonly employed in the preparation of protease inhibitors and kinase inhibitors due to the functional groups that enable further derivatization. Widely utilized in medicinal chemistry for structure-activity relationship (SAR) studies.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿6,510.00
250mg
10-20 days ฿10,610.00
1g
10-20 days ฿29,870.00
(3R,4R)-tert-Butyl 3-bromo-4-hydroxypyrrolidine-1-carboxylate
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Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of antiviral and antidiabetic drugs. Its stereochemistry allows for selective reactions in multi-step organic syntheses, making it valuable in constructing complex molecules with high enantiomeric purity. Commonly employed in the preparation of protease inhibitors and kinase inhibitors due to the functional groups that enable further derivatization. Widely utilized in medicinal chemistry for struc

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of antiviral and antidiabetic drugs. Its stereochemistry allows for selective reactions in multi-step organic syntheses, making it valuable in constructing complex molecules with high enantiomeric purity. Commonly employed in the preparation of protease inhibitors and kinase inhibitors due to the functional groups that enable further derivatization. Widely utilized in medicinal chemistry for structure-activity relationship (SAR) studies.

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