(S)-tert-Butyl 2-((methylamino)methyl)pyrrolidine-1-carboxylate

≥95%

Reagent Code: #71108
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CAS Number 191231-58-0

science Other reagents with same CAS 191231-58-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.31 g/mol
Formula C₁₁H₂₂N₂O₂
badge Registry Numbers
MDL Number MFCD07786221
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive molecules. Its structure, featuring a pyrrolidine ring and a tert-butyl carboxylate group, makes it a valuable building block for the development of chiral compounds, particularly in the production of drugs targeting neurological and cardiovascular disorders. Additionally, it is employed in the creation of ligands for asymmetric catalysis, aiding in the efficient synthesis of enantiomerically pure substances. Its application extends to research settings, where it is used to explore new chemical reactions and pathways in organic synthesis.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿12,483.00
inventory 100mg
10-20 days ฿7,776.00
inventory 1g
10-20 days ฿31,302.00

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(S)-tert-Butyl 2-((methylamino)methyl)pyrrolidine-1-carboxylate
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This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive molecules. Its structure, featuring a pyrrolidine ring and a tert-butyl carboxylate group, makes it a valuable building block for the development of chiral compounds, particularly in the production of drugs targeting neurological and cardiovascular disorders. Additionally, it is employed in the creation of ligands for asymmetric catalysis, aiding in the efficient synthesis of ena

This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive molecules. Its structure, featuring a pyrrolidine ring and a tert-butyl carboxylate group, makes it a valuable building block for the development of chiral compounds, particularly in the production of drugs targeting neurological and cardiovascular disorders. Additionally, it is employed in the creation of ligands for asymmetric catalysis, aiding in the efficient synthesis of enantiomerically pure substances. Its application extends to research settings, where it is used to explore new chemical reactions and pathways in organic synthesis.

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