trans-tert-Butyl 3-(Hydroxymethyl)-4-methylpyrrolidine-1-carboxylate

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Reagent Code: #71318
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CAS Number 1349715-96-3

science Other reagents with same CAS 1349715-96-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.29 g/mol
Formula C₁₁H₂₁NO₃
badge Registry Numbers
MDL Number MFCD02179042
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis as an intermediate in the production of more complex molecules, particularly in pharmaceutical research. Its structure, featuring a pyrrolidine ring with hydroxyl and carboxylate groups, makes it a versatile building block for the development of bioactive compounds. It is often employed in the synthesis of potential drug candidates, especially those targeting neurological or cardiovascular disorders. Additionally, its tert-butyl group provides steric protection, enhancing selectivity in chemical reactions. This compound is also used in the preparation of chiral ligands for asymmetric catalysis, aiding in the creation of enantiomerically pure substances.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿19,206.00
inventory 250mg
10-20 days ฿7,686.00

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trans-tert-Butyl 3-(Hydroxymethyl)-4-methylpyrrolidine-1-carboxylate
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This compound is primarily utilized in organic synthesis as an intermediate in the production of more complex molecules, particularly in pharmaceutical research. Its structure, featuring a pyrrolidine ring with hydroxyl and carboxylate groups, makes it a versatile building block for the development of bioactive compounds. It is often employed in the synthesis of potential drug candidates, especially those targeting neurological or cardiovascular disorders. Additionally, its tert-butyl group provides ster

This compound is primarily utilized in organic synthesis as an intermediate in the production of more complex molecules, particularly in pharmaceutical research. Its structure, featuring a pyrrolidine ring with hydroxyl and carboxylate groups, makes it a versatile building block for the development of bioactive compounds. It is often employed in the synthesis of potential drug candidates, especially those targeting neurological or cardiovascular disorders. Additionally, its tert-butyl group provides steric protection, enhancing selectivity in chemical reactions. This compound is also used in the preparation of chiral ligands for asymmetric catalysis, aiding in the creation of enantiomerically pure substances.

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