tert-Butyl hydroxy(methyl)carbamate

97%

Reagent Code: #148467
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CAS Number 19689-97-5

science Other reagents with same CAS 19689-97-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 147.17 g/mol
Formula C₆H₁₃NO₃
badge Registry Numbers
MDL Number MFCD24465554
thermostat Physical Properties
Boiling Point 192.7°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.083g/cm3
Storage 2-8°C, dry seal

description Product Description

Used as a protecting group in organic synthesis, particularly for amines. The tert-butyl hydroxy(methyl)carbamate moiety helps mask reactive amine functionalities during multi-step reactions, allowing selective transformations elsewhere in the molecule. It is stable under a variety of reaction conditions but can be removed under mild acidic conditions, making it valuable in peptide synthesis and pharmaceutical development. Its hydroxyl group also allows for further functionalization or attachment to solid supports in combinatorial chemistry.

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Test Parameter Specification
Appearance Liquid
Purity (%) 96.5-100%
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿960.00
inventory 1g
10-20 days ฿1,800.00
inventory 5g
10-20 days ฿5,560.00

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tert-Butyl hydroxy(methyl)carbamate
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Used as a protecting group in organic synthesis, particularly for amines. The tert-butyl hydroxy(methyl)carbamate moiety helps mask reactive amine functionalities during multi-step reactions, allowing selective transformations elsewhere in the molecule. It is stable under a variety of reaction conditions but can be removed under mild acidic conditions, making it valuable in peptide synthesis and pharmaceutical development. Its hydroxyl group also allows for further functionalization or attachment to solid s
Used as a protecting group in organic synthesis, particularly for amines. The tert-butyl hydroxy(methyl)carbamate moiety helps mask reactive amine functionalities during multi-step reactions, allowing selective transformations elsewhere in the molecule. It is stable under a variety of reaction conditions but can be removed under mild acidic conditions, making it valuable in peptide synthesis and pharmaceutical development. Its hydroxyl group also allows for further functionalization or attachment to solid supports in combinatorial chemistry.
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