tert-Butyl (1-hydroxy-3-methoxypropan-2-yl)carbamate

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Reagent Code: #87911
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CAS Number 1334171-66-2

science Other reagents with same CAS 1334171-66-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.25 g/mol
Formula C₉H₁₉NO₄
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MDL Number MFCD20261173
inventory_2 Storage & Handling
Storage 2-8°C, inert gas

description Product Description

This chemical is primarily used in organic synthesis as a protecting group for amines. It is particularly valuable in peptide synthesis, where it helps to prevent unwanted reactions at the amine group during the formation of peptide bonds. The tert-butyl group provides stability under various reaction conditions, while the hydroxy and methoxy groups offer additional functional handles for further modifications. Its application extends to the preparation of complex molecules in pharmaceutical research, where selective protection and deprotection of functional groups are crucial. Additionally, it can be employed in the development of prodrugs, where controlled release of active pharmaceutical ingredients is required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿22,815.00

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tert-Butyl (1-hydroxy-3-methoxypropan-2-yl)carbamate
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This chemical is primarily used in organic synthesis as a protecting group for amines. It is particularly valuable in peptide synthesis, where it helps to prevent unwanted reactions at the amine group during the formation of peptide bonds. The tert-butyl group provides stability under various reaction conditions, while the hydroxy and methoxy groups offer additional functional handles for further modifications. Its application extends to the preparation of complex molecules in pharmaceutical research, wh

This chemical is primarily used in organic synthesis as a protecting group for amines. It is particularly valuable in peptide synthesis, where it helps to prevent unwanted reactions at the amine group during the formation of peptide bonds. The tert-butyl group provides stability under various reaction conditions, while the hydroxy and methoxy groups offer additional functional handles for further modifications. Its application extends to the preparation of complex molecules in pharmaceutical research, where selective protection and deprotection of functional groups are crucial. Additionally, it can be employed in the development of prodrugs, where controlled release of active pharmaceutical ingredients is required.

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