N-Benzylpyrrolidine-2-carboxamide hydrochloride

95%

Reagent Code: #215878
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CAS Number 1236255-21-2

science Other reagents with same CAS 1236255-21-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 240.73 g/mol
Formula C₁₂H₁₇ClN₂O
badge Registry Numbers
MDL Number MFCD13562760
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and enzyme inhibitors. Its structure supports the design of compounds with high selectivity and binding affinity, making it valuable in medicinal chemistry research. Commonly employed in the preparation of bioactive molecules where the pyrrolidine ring acts as a conformational constraint. Also utilized in the creation of chiral building blocks for asymmetric synthesis.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿3,920.00
250mg
10-20 days ฿6,650.00
1g
10-20 days ฿17,960.00
N-Benzylpyrrolidine-2-carboxamide hydrochloride
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and enzyme inhibitors. Its structure supports the design of compounds with high selectivity and binding affinity, making it valuable in medicinal chemistry research. Commonly employed in the preparation of bioactive molecules where the pyrrolidine ring acts as a conformational constraint. Also utilized in the creation of chiral building blocks for asymmetric synthesis.

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and enzyme inhibitors. Its structure supports the design of compounds with high selectivity and binding affinity, making it valuable in medicinal chemistry research. Commonly employed in the preparation of bioactive molecules where the pyrrolidine ring acts as a conformational constraint. Also utilized in the creation of chiral building blocks for asymmetric synthesis.

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