Methyl 2-(tert-Butoxycarbonylamino)-3-nitrobenzoate
≥98%
Reagent
Code: #115879
CAS Number
57113-90-3
blur_circular Chemical Specifications
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Molecular Information
Weight
296.28 g/mol
Formula
C₁₃H₁₆N₂O₆
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Registry Numbers
MDL Number
MFCD06797690
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Physical Properties
Melting Point
104-108°C
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Storage & Handling
Storage
room temperature
description Product Description
This chemical is primarily used in organic synthesis as an intermediate for the preparation of more complex molecules. It is particularly valuable in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs). The tert-butoxycarbonyl (Boc) group serves as a protective group for amines, allowing selective reactions to occur at other sites of the molecule without interference. The nitro group can be reduced to an amine, which can then be further functionalized, making it useful in the synthesis of various heterocyclic compounds. Additionally, its ester group can be hydrolyzed to yield carboxylic acids, which are versatile intermediates in medicinal chemistry. This compound is often employed in the synthesis of peptidomimetics and other bioactive molecules, contributing to drug discovery and development processes.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | White To Very Pale Yellow To Yellow To Green Powder To Crystal |
Purity (%) | 97.5-100 |
Infrared Spectrum | Conforms To Structure |
NMR | Conforms To Structure |
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Methyl 2-(tert-Butoxycarbonylamino)-3-nitrobenzoate
This chemical is primarily used in organic synthesis as an intermediate for the preparation of more complex molecules. It is particularly valuable in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs). The tert-butoxycarbonyl (Boc) group serves as a protective group for amines, allowing selective reactions to occur at other sites of the molecule without interference. The nitro group can be reduced to an amine, which can then be further functionalized, making it useful in the synthesis of various heterocyclic compounds. Additionally, its ester group can be hydrolyzed to yield carboxylic acids, which are versatile intermediates in medicinal chemistry. This compound is often employed in the synthesis of peptidomimetics and other bioactive molecules, contributing to drug discovery and development processes.
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