tert-Butyl ((1R,3S)-3-hydroxycyclopentyl)carbamate

97%

Reagent Code: #112977
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CAS Number 225641-84-9

science Other reagents with same CAS 225641-84-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.26 g/mol
Formula C₁₀H₁₉NO₃
badge Registry Numbers
MDL Number MFCD18791196
thermostat Physical Properties
Boiling Point 320.8°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of drugs targeting neurological and cardiovascular conditions. Its structure, featuring a cyclopentyl ring and a carbamate group, makes it a valuable building block in organic synthesis. It is often employed in the preparation of chiral molecules, where its stereochemistry plays a crucial role in achieving the desired biological activity. Additionally, it is used in research settings to study enzyme interactions and receptor binding, aiding in the discovery of new therapeutic agents. Its stability and reactivity also make it suitable for use in peptide coupling reactions and as a protective group in complex organic transformations.

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Test Parameter Specification
Appearance White To Off-White Solid
Purity (%) 96.5-100%
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,860.00
inventory 250mg
10-20 days ฿5,950.00
inventory 1g
10-20 days ฿15,510.00

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tert-Butyl ((1R,3S)-3-hydroxycyclopentyl)carbamate
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This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of drugs targeting neurological and cardiovascular conditions. Its structure, featuring a cyclopentyl ring and a carbamate group, makes it a valuable building block in organic synthesis. It is often employed in the preparation of chiral molecules, where its stereochemistry plays a crucial role in achieving the desired biological activity. Additionally, it is used in research settings to study enzyme interactions and receptor binding, aiding in the discovery of new therapeutic agents. Its stability and reactivity also make it suitable for use in peptide coupling reactions and as a protective group in complex organic transformations.
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