Methyl 2-(tert-Butoxycarbonylamino)-3-nitrobenzoate

≥98%

Reagent Code: #115879
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CAS Number 57113-90-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 296.28 g/mol
Formula C₁₃H₁₆N₂O₆
badge Registry Numbers
MDL Number MFCD06797690
thermostat Physical Properties
Melting Point 104-108°C
inventory_2 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.

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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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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿4,920.00
inventory 1g
10-20 days ฿1,850.00
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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