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

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Reagent Code: #126382
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CAS Number 1190890-11-9

science Other reagents with same CAS 1190890-11-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.74 g/mol
Formula C10H21ClN2O2
badge Registry Numbers
MDL Number MFCD11101392
inventory_2 Storage & Handling
Storage room temperature, inert gas

description Product Description

This compound is primarily used in pharmaceutical research and development as a chiral building block for the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring a pyrrolidine ring and a protected amine group, makes it valuable in the preparation of compounds with potential biological activity, particularly in the fields of neuroscience and oncology. It is often employed in asymmetric synthesis to create enantiomerically pure molecules, which are crucial for developing drugs with high specificity and reduced side effects. Additionally, it serves as an intermediate in the production of peptidomimetics and other bioactive molecules, contributing to advancements in drug discovery and medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,400.00
inventory 250mg
10-20 days ฿5,950.00
inventory 1g
10-20 days ฿23,750.00

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(S)-tert-Butyl 2-(aminomethyl)pyrrolidine-1-carboxylate hydrochloride
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This compound is primarily used in pharmaceutical research and development as a chiral building block for the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring a pyrrolidine ring and a protected amine group, makes it valuable in the preparation of compounds with potential biological activity, particularly in the fields of neuroscience and oncology. It is often employed in asymmetric synthesis to create enantiomerically pure molecules, which are crucial for developing drugs with high specificity and reduced side effects. Additionally, it serves as an intermediate in the production of peptidomimetics and other bioactive molecules, contributing to advancements in drug discovery and medicinal chemistry.
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