(2R,4S)-tert-Butyl 4-amino-2-methylpyrrolidine-1-carboxylate

98%

Reagent Code: #230826
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CAS Number 348165-60-6

science Other reagents with same CAS 348165-60-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.28 g/mol
Formula C₁₀H₂₀N₂O₂
badge Registry Numbers
MDL Number MFCD27988061
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and antiviral drugs. Its stereochemistry allows for selective binding in biological systems, making it valuable in creating enantiomerically pure compounds. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the stability and modifiability of the pyrrolidine scaffold. Also utilized in the preparation of bioactive molecules where amine functionality can be acylated or alkylated to form amide or tertiary amine derivatives.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿8,040.00
250mg
10-20 days ฿16,030.00
1g
10-20 days ฿40,130.00
(2R,4S)-tert-Butyl 4-amino-2-methylpyrrolidine-1-carboxylate
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Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and antiviral drugs. Its stereochemistry allows for selective binding in biological systems, making it valuable in creating enantiomerically pure compounds. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the stability and modifiability of the pyrrolidine scaffold. Also utilized in the preparation of bioactive molecules where

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and antiviral drugs. Its stereochemistry allows for selective binding in biological systems, making it valuable in creating enantiomerically pure compounds. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the stability and modifiability of the pyrrolidine scaffold. Also utilized in the preparation of bioactive molecules where amine functionality can be acylated or alkylated to form amide or tertiary amine derivatives.

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