2-(4-Nitrobenzamido)pentanedioic acid

95%

Reagent Code: #130256
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CAS Number 22536-03-4

science Other reagents with same CAS 22536-03-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 296.23 g/mol
Formula C₁₂H₁₂N₂O₇
badge Registry Numbers
MDL Number MFCD00066818
thermostat Physical Properties
Melting Point 114-116 °C
Boiling Point 619.9±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.501±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its carboxylic acid groups allow conjugation with amines or alcohols, making it useful in peptide-like structure formation. The nitrobenzamide moiety can be reduced to an aniline derivative, enabling further functionalization for drug development. Also employed in the preparation of enzyme inhibitors or receptor ligands due to its ability to mimic dicarboxylic acid-containing biomolecules. Suitable for research in medicinal chemistry and molecular design.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,760.00
inventory 5g
10-20 days ฿14,880.00
inventory 1g
10-20 days ฿4,660.00

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2-(4-Nitrobenzamido)pentanedioic acid
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Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its carboxylic acid groups allow conjugation with amines or alcohols, making it useful in peptide-like structure formation. The nitrobenzamide moiety can be reduced to an aniline derivative, enabling further functionalization for drug development. Also employed in the preparation of enzyme inhibitors or receptor ligands due to its ability to mimic dicarboxylic acid-containing biomolecules. Suitable for research in m

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its carboxylic acid groups allow conjugation with amines or alcohols, making it useful in peptide-like structure formation. The nitrobenzamide moiety can be reduced to an aniline derivative, enabling further functionalization for drug development. Also employed in the preparation of enzyme inhibitors or receptor ligands due to its ability to mimic dicarboxylic acid-containing biomolecules. Suitable for research in medicinal chemistry and molecular design.

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