3-Benzoylbenzoic acid (CAS 579-18-0)
QUICK LINKS
3-Benzoylbenzoic acid is a compound that functions as a key intermediate in the synthesis of various organic compounds. It acts as a precursor in the production of dyes, and other chemicals. Its mode of action involves participating in Friedel-Crafts acylation reactions, where it serves as an acylating agent to introduce the benzoyl group into aromatic compounds. 3-Benzoylbenzoic acid plays a role in the formation of complex organic molecules by facilitating the attachment of the benzoyl group to specific positions on the aromatic ring. This process is for the development of diverse chemical compounds with unique properties and functionalities. 3-Benzoylbenzoic acid is involved in the synthesis of advanced materials and serves as a building block for the creation of novel chemical structures with potential applications in various fields.
3-Benzoylbenzoic acid (CAS 579-18-0) References
- An electrogenerated poly(pyrrole-benzophenone) film for the photografting of proteins. | Cosnier, S. and Senillou, A. 2003. Chem Commun (Camb). 414-5. PMID: 12613639
- Exploring the ability of frozen-density embedding to model induced circular dichroism. | Neugebauer, J. and Baerends, EJ. 2006. J Phys Chem A. 110: 8786-96. PMID: 16836441
- Photografting and patterning of oligonucleotides on benzophenone-modified boron-doped diamond. | Szunerits, S., et al. 2007. Chem Commun (Camb). 2793-5. PMID: 17609778
- Simple inhibitors of histone deacetylase activity that combine features of short-chain fatty acid and hydroxamic acid inhibitors. | Tischler, JL., et al. 2008. J Enzyme Inhib Med Chem. 23: 549-55. PMID: 18608778
- Photochemical immobilization of proteins and peptides on benzophenone-terminated boron-doped diamond surfaces. | Marcon, L., et al. 2010. Langmuir. 26: 1075-80. PMID: 19821607
- Application of complementary mass spectrometric techniques to the identification of ketoprofen phototransformation products. | Kosjek, T., et al. 2011. J Mass Spectrom. 46: 391-401. PMID: 21438089
- Differentiation of regioisomeric aromatic ketocarboxylic acids by positive mode atmospheric pressure chemical ionization collision-activated dissociation tandem mass spectrometry in a linear quadrupole ion trap mass spectrometer. | Amundson, LM., et al. 2011. J Am Soc Mass Spectrom. 22: 670-82. PMID: 21472606
- Sunlight-driven copper-catalyst activation applied to photolatent click chemistry. | Beniazza, R., et al. 2014. Chemistry. 20: 13181-7. PMID: 25171758
- Effective ascorbate-free and photolatent click reactions in water using a photoreducible copper(II)-ethylenediamine precatalyst. | Beniazza, R., et al. 2015. Beilstein J Org Chem. 11: 1950-9. PMID: 26664615
- Purification, characterization, and properties of an aryl aldehyde oxidoreductase from Nocardia sp. strain NRRL 5646. | Li, T. and Rosazza, JP. 1997. J Bacteriol. 179: 3482-7. PMID: 9171390
- A mechanistic study of polybenzoxazole formation with model compounds | Ying-Hung So, Jerry P. Heeschen, and Cheryl L. Murlick. 1995. Macromolecules., 28, 21,: 7289–7290.
- First Atropo-Enantioselective Ring Opening of Achiral Biaryls Containing Lactone Bridges with Chiral Hydride-Transfer Reagents Derived from Borane†‡ | and Prof. Dr. Gerhard Bringmann, Dipl.-Chem. Thomas Hartung. Issue6 June 1992. Angewandte Chemie International Edition in English. Volume31,: Pages 761-762.
- Synthesis of flavonol derivatives as probes of biological processes | and H Tanaka, MM Stohlmeyer, TJ Wandless, LP Taylor - Tetrahedron Letters, 2000 - Elsevier. 9 December 2000,. Tetrahedron Letters. Volume 41, Issue 50,: Pages 9735-9739.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
3-Benzoylbenzoic acid, 5 g | sc-231477 | 5 g | $52.00 |