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

≥95%

Reagent Code: #70903
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CAS Number 1400562-12-0

science Other reagents with same CAS 1400562-12-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.28 g/mol
Formula C₁₀H₂₀N₂O₃
badge Registry Numbers
MDL Number MFCD20230534
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various biologically active compounds. Its structure, featuring both amino and methoxy groups, makes it a valuable building block for the development of drugs targeting neurological and cardiovascular disorders. Specifically, it is often employed in the preparation of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) agents, where its stereochemistry plays a critical role in enhancing drug efficacy and selectivity. Additionally, its tert-butyl carbamate group provides stability during synthetic processes, making it a preferred choice for multi-step organic syntheses.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,403.00
inventory 250mg
10-20 days ฿22,815.00

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(3R,4R)-tert-Butyl 3-amino-4-methoxypyrrolidine-1-carboxylate
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This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various biologically active compounds. Its structure, featuring both amino and methoxy groups, makes it a valuable building block for the development of drugs targeting neurological and cardiovascular disorders. Specifically, it is often employed in the preparation of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) agents, where its stereochemistry plays a critical role in enhancing drug efficacy and selectivity. Additionally, its tert-butyl carbamate group provides stability during synthetic processes, making it a preferred choice for multi-step organic syntheses.
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