tert-Butyl (2-hydroxycyclopentyl)carbamate

95%

Reagent Code: #36452
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CAS Number 945652-35-7

science Other reagents with same CAS 945652-35-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.2628 g/mol
Formula C₁₀H₁₉NO₃
badge Registry Numbers
MDL Number MFCD09261198
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

tert-Butyl (2-hydroxycyclopentyl)carbamate is primarily used in organic synthesis as an intermediate for the preparation of more complex chemical compounds. Its structure, featuring both a carbamate group and a hydroxyl group, makes it a versatile building block in the development of pharmaceuticals, particularly in the synthesis of bioactive molecules. The compound is often employed in the creation of cyclopentane-based scaffolds, which are valuable in drug discovery for their potential therapeutic properties. Additionally, it can serve as a protective group for amines during multi-step synthetic processes, enabling selective reactions in the presence of other functional groups. Its stability and reactivity make it a useful reagent in medicinal chemistry and material science research.

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inventory 100mg
10-20 days ฿7,020.00

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tert-Butyl (2-hydroxycyclopentyl)carbamate
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tert-Butyl (2-hydroxycyclopentyl)carbamate is primarily used in organic synthesis as an intermediate for the preparation of more complex chemical compounds. Its structure, featuring both a carbamate group and a hydroxyl group, makes it a versatile building block in the development of pharmaceuticals, particularly in the synthesis of bioactive molecules. The compound is often employed in the creation of cyclopentane-based scaffolds, which are valuable in drug discovery for their potential therapeutic prop

tert-Butyl (2-hydroxycyclopentyl)carbamate is primarily used in organic synthesis as an intermediate for the preparation of more complex chemical compounds. Its structure, featuring both a carbamate group and a hydroxyl group, makes it a versatile building block in the development of pharmaceuticals, particularly in the synthesis of bioactive molecules. The compound is often employed in the creation of cyclopentane-based scaffolds, which are valuable in drug discovery for their potential therapeutic properties. Additionally, it can serve as a protective group for amines during multi-step synthetic processes, enabling selective reactions in the presence of other functional groups. Its stability and reactivity make it a useful reagent in medicinal chemistry and material science research.

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