tert-butyl N-[(1S,2S)-2-hydroxycyclopentyl]carbamate

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Reagent Code: #122374
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CAS Number 145106-43-0

science Other reagents with same CAS 145106-43-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.26 g/mol
Formula CH₁₉NO₃
badge Registry Numbers
MDL Number MFCD11656038
inventory_2 Storage & Handling
Storage Room temperature, airtight, dry

description Product Description

This compound is primarily utilized in organic synthesis as a chiral building block for the preparation of more complex molecules. Its structure, featuring a cyclopentyl ring with hydroxyl and carbamate functional groups, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of enantiomerically pure drugs. It is often employed in the construction of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Additionally, it serves as a protective group for amines during multi-step synthetic processes, ensuring selective reactivity in the presence of other functional groups. Its stability and ease of deprotection make it a practical choice in medicinal chemistry and drug discovery.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,260.00
inventory 250mg
10-20 days ฿648.00
inventory 5g
10-20 days ฿4,419.00

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tert-butyl N-[(1S,2S)-2-hydroxycyclopentyl]carbamate
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This compound is primarily utilized in organic synthesis as a chiral building block for the preparation of more complex molecules. Its structure, featuring a cyclopentyl ring with hydroxyl and carbamate functional groups, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of enantiomerically pure drugs. It is often employed in the construction of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Additionally, i

This compound is primarily utilized in organic synthesis as a chiral building block for the preparation of more complex molecules. Its structure, featuring a cyclopentyl ring with hydroxyl and carbamate functional groups, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of enantiomerically pure drugs. It is often employed in the construction of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Additionally, it serves as a protective group for amines during multi-step synthetic processes, ensuring selective reactivity in the presence of other functional groups. Its stability and ease of deprotection make it a practical choice in medicinal chemistry and drug discovery.

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