(S)-2-(((tert-Butyldimethylsilyl)oxy)methyl)pyrrolidine

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Reagent Code: #38059
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CAS Number 134756-75-5

science Other reagents with same CAS 134756-75-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.41 g/mol
Formula C₁₁H₂₅NOSi
badge Registry Numbers
MDL Number MFCD11502840
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in an inert gas

description Product Description

This chemical is primarily utilized in organic synthesis as a chiral building block or intermediate. It is often employed in the preparation of pharmaceuticals, particularly in the synthesis of enantiomerically pure compounds. The tert-butyldimethylsilyl (TBDMS) group serves as a protective group for hydroxyl functionalities, ensuring selective reactions can occur at other sites of the molecule. Its chiral nature makes it valuable in the development of drugs and bioactive molecules where stereochemistry plays a critical role in efficacy. Additionally, it is used in the synthesis of complex natural products and in asymmetric catalysis to achieve high enantioselectivity in reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,917.00
inventory 250mg
10-20 days ฿3,825.00

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(S)-2-(((tert-Butyldimethylsilyl)oxy)methyl)pyrrolidine
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This chemical is primarily utilized in organic synthesis as a chiral building block or intermediate. It is often employed in the preparation of pharmaceuticals, particularly in the synthesis of enantiomerically pure compounds. The tert-butyldimethylsilyl (TBDMS) group serves as a protective group for hydroxyl functionalities, ensuring selective reactions can occur at other sites of the molecule. Its chiral nature makes it valuable in the development of drugs and bioactive molecules where stereochemistry

This chemical is primarily utilized in organic synthesis as a chiral building block or intermediate. It is often employed in the preparation of pharmaceuticals, particularly in the synthesis of enantiomerically pure compounds. The tert-butyldimethylsilyl (TBDMS) group serves as a protective group for hydroxyl functionalities, ensuring selective reactions can occur at other sites of the molecule. Its chiral nature makes it valuable in the development of drugs and bioactive molecules where stereochemistry plays a critical role in efficacy. Additionally, it is used in the synthesis of complex natural products and in asymmetric catalysis to achieve high enantioselectivity in reactions.

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