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2,3-Diaminobenzoic acid (CAS 603-81-6)

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Alternate Names:
3-Carboxy-1,2-diaminobenzene
Application:
2,3-Diaminobenzoic acid is an aromatic building block
CAS Number:
603-81-6
Molecular Weight:
152.15
Molecular Formula:
C7H8N2O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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2,3-Diaminobenzoic acid is a compound that functions as a building block in the synthesis of various organic molecules. It may play a role in the formation of polymers and coordination complexes, contributing to the development of new materials and compounds. At the molecular level, 2,3-Diaminobenzoic acid interacts with other reagents to form specific chemical bonds, enabling the creation of complex structures with tailored properties. Its mechanism of action involves participating in chemical reactions that lead to the production of diverse compounds with potential applications in materials science and chemical engineering. 2,3-Diaminobenzoic Acid′s function lies in its ability to contribute to the synthesis of novel materials and compounds, expanding the range of available substances for various industrial and scientific purposes.


2,3-Diaminobenzoic acid (CAS 603-81-6) References

  1. Resistance-modifying agents. 9. Synthesis and biological properties of benzimidazole inhibitors of the DNA repair enzyme poly(ADP-ribose) polymerase.  |  White, AW., et al. 2000. J Med Chem. 43: 4084-97. PMID: 11063605
  2. On benzo[b][1,4]diazepinium-olates, -thiolates and -carboxylates as anti-Hückel mesomeric betaines.  |  Schmidt, A., et al. 2003. Org Biomol Chem. 1: 4342-50. PMID: 14685339
  3. Characterization of the antiallergic drugs 3-[2-(2-phenylethyl) benzoimidazole-4-yl]-3-hydroxypropanoic acid and ethyl 3-hydroxy-3-[2-(2-phenylethyl)benzoimidazol-4-yl]propanoate as full aryl hydrocarbon receptor agonists.  |  Morales, JL., et al. 2008. Chem Res Toxicol. 21: 472-82. PMID: 18179178
  4. Biosynthesis of aurachins A-L in Stigmatella aurantiaca: a feeding study.  |  Höfle, G. and Kunze, B. 2008. J Nat Prod. 71: 1843-9. PMID: 18989924
  5. Catalytic oxidation of o-aminophenols and aromatic amines by mushroom tyrosinase.  |  Muñoz-Muñoz, JL., et al. 2011. Biochim Biophys Acta. 1814: 1974-83. PMID: 21810487
  6. Kinetic characterisation of o-aminophenols and aromatic o-diamines as suicide substrates of tyrosinase.  |  Muñoz-Muñoz, JL., et al. 2012. Biochim Biophys Acta. 1824: 647-55. PMID: 22342555
  7. Direct Photochemical C-H Carboxylation of Aromatic Diamines with CO2 under Electron-Donor- and Base-free Conditions.  |  Matsumoto, T., et al. 2018. Sci Rep. 8: 14623. PMID: 30279606
  8. Modification-Free Fabricating Ratiometric Nanoprobe Based on Dual-Emissive Carbon Dots for Nitrite Determination in Food Samples.  |  Liu, J., et al. 2019. J Agric Food Chem. 67: 3826-3836. PMID: 30848591
  9. Synthesis of Some Benzimidazole-derived Molecules and their Effects on PARP-1 Activity and MDA-MB-231, MDA-MB-436, MDA-MB-468 Breast Cancer Cell Viability.  |  Gurkan-Alp, AS., et al. 2020. Anticancer Agents Med Chem. 20: 1728-1738. PMID: 32357823
  10. A High-Throughput Screening Method for Determining the Optimized Synthesis Conditions of Quinoxaline Derivatives Using Microdroplet Reaction.  |  Yang, Y., et al. 2020. Front Chem. 8: 789. PMID: 33195024
  11. Secondary Effects of Hypochlorite Treatment on the Emerging Pollutant Candesartan: The Formation of Degradation Byproducts and Their Toxicological Profiles.  |  Luongo, G., et al. 2021. Molecules. 26: PMID: 34198752
  12. Novel Rivastigmine Derivatives as Promising Multi-Target Compounds for Potential Treatment of Alzheimer's Disease.  |  Vicente-Zurdo, D., et al. 2022. Biomedicines. 10: PMID: 35884815
  13. Macromolecule synthesis and breakdown in relation to sporulation and meiosis in yeast.  |  Hopper, AK., et al. 1974. J Bacteriol. 119: 619-28. PMID: 4604714

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2,3-Diaminobenzoic acid, 1 g

sc-275242
1 g
$35.00