(R)-tert-Butyl 2-(aminomethyl)pyrrolidine-1-carboxylate hydrochloride

≥95%

Reagent Code: #230973
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CAS Number 1190890-12-0

science Other reagents with same CAS 1190890-12-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.74 g/mol
Formula C₁₀H₂₁ClN₂O₂
badge Registry Numbers
MDL Number MFCD11101385
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Widely used in pharmaceutical synthesis, this compound serves as a key chiral intermediate in the production of active pharmaceutical ingredients (APIs), particularly in the development of protease inhibitors and other biologically active molecules. Its protected amine and chiral pyrrolidine backbone make it ideal for asymmetric synthesis and selective transformations in multi-step drug manufacturing. It is frequently employed in the preparation of antiviral and anticancer agents due to its structural compatibility with enzyme-targeting therapeutics. Additionally, its solubility and stability as a hydrochloride salt facilitate handling and coupling reactions in both research and industrial settings.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿3,870.00
250mg
10-20 days ฿8,590.00
1g
10-20 days ฿30,000.00
(R)-tert-Butyl 2-(aminomethyl)pyrrolidine-1-carboxylate hydrochloride
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Widely used in pharmaceutical synthesis, this compound serves as a key chiral intermediate in the production of active pharmaceutical ingredients (APIs), particularly in the development of protease inhibitors and other biologically active molecules. Its protected amine and chiral pyrrolidine backbone make it ideal for asymmetric synthesis and selective transformations in multi-step drug manufacturing. It is frequently employed in the preparation of antiviral and anticancer agents due to its structural co

Widely used in pharmaceutical synthesis, this compound serves as a key chiral intermediate in the production of active pharmaceutical ingredients (APIs), particularly in the development of protease inhibitors and other biologically active molecules. Its protected amine and chiral pyrrolidine backbone make it ideal for asymmetric synthesis and selective transformations in multi-step drug manufacturing. It is frequently employed in the preparation of antiviral and anticancer agents due to its structural compatibility with enzyme-targeting therapeutics. Additionally, its solubility and stability as a hydrochloride salt facilitate handling and coupling reactions in both research and industrial settings.

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