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![Benzo[c]cinnoline (CAS 230-17-1) - chemical structure image](https://media.scbt.com/product/benzoccinnoline-230-17-1-structure_19_51_t_195101.jpg "Molecular structure of Benzo[c]cinnoline, CAS Number: 230-17-1")
Benzo[c]cinnoline (CAS 230-17-1)
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Benzo[c]cinnoline, alternatively known as 1,2,3,4-tetrahydro-1,4-dioxino[2,3-b]benzofuran, serves as an organic heterocyclic compound that finds extensive utility as an intermediate in the synthesis of dyes and other compounds. This compound is characterized by a six-membered ring composed of five carbon atoms and one nitrogen atom. The applications of Benzo[c]cinnoline span across several fields, including organic synthesis and material science. Within organic synthesis, it finds usage in the synthesis of dyes, pigments, and other compounds. In the realm of organic synthesis, Benzo[c]cinnoline serves as a vital precursor for the creation of amino acids, peptides, and nucleotides. Additionally, it holds significance within material science, acting as a fundamental building block for the synthesis of polymers and various other materials.
Benzo[c]cinnoline (CAS 230-17-1) References
- Investigations of a novel process to the framework of benzo[c]cinnoline. | Bjørsvik, HR., et al. 2004. J Org Chem. 69: 7720-7. PMID: 15498002
- The reactivity patterns of low-coordinate iron-hydride complexes. | Yu, Y., et al. 2008. J Am Chem Soc. 130: 6624-38. PMID: 18444648
- Selective formation of benzo[c]cinnoline by photocatalytic reduction of 2,2'-dinitrobiphenyl using TiO2 and under UV light irradiation. | Kaur, J. and Pal, B. 2015. Chem Commun (Camb). 51: 8500-3. PMID: 25891261
- Reduction of ((t)BuN═)NbCl3(py)2 in a Salt-Free Manner for Generating Nb(IV) Dinuclear Complexes and Their Reactivity toward Benzo[c]cinnoline. | Saito, T., et al. 2015. Inorg Chem. 54: 6004-9. PMID: 26017157
- Elucidating the Mechanism of Uranium Mediated Diazene N═N Bond Cleavage. | Kiernicki, JJ., et al. 2016. Inorg Chem. 55: 11854-11866. PMID: 27805393
- Isomer Dependence on the Reactivity of Diazenes with Pentaphenylborole. | Adiraju, VAK. and Martin, CD. 2017. Chemistry. 23: 11437-11444. PMID: 28675467
- Theoretical investigation on hydrogen bond interaction of diketo/keto-enol form uracil and thymine tautomers with intercalators. | Anithaa, VS., et al. 2017. J Mol Model. 23: 333. PMID: 29105034
- The Hydrazine-O2 Redox Couple as a Platform for Organocatalytic Oxidation: Benzo[c]cinnoline-Catalyzed Oxidation of Alkyl Halides to Aldehydes. | Stone, IB., et al. 2018. Angew Chem Int Ed Engl. 57: 12494-12498. PMID: 30016572
- A Dimeric Chromium(II) Pincer as an Electron Shuttle for N=N Bond Scission. | Labrum, NS., et al. 2020. Chemistry. 26: 13915-13926. PMID: 32428366
- 2-Amino-3'-dialkylaminobiphenyl-based fluorescent intracellular probes for nitric oxide surrogate N2O3. | Escamilla, PR., et al. 2020. Chem Sci. 11: 1394-1403. PMID: 34123264
- N═N Bond Cleavage by Tantalum Hydride Complexes: Mechanistic Insights and Reactivity. | Álvarez-Ruiz, E., et al. 2022. Inorg Chem. 61: 474-485. PMID: 34890181
- Electrochemical Strategy for Proton Relay Installation Enhances the Activity of a Hydrogen Evolution Electrocatalyst. | Lin, S., et al. 2022. J Am Chem Soc. 144: 20267-20277. PMID: 36305871
- Reaction between benzo[c]cinnoline and dimethyl acetylenedicarboxylate. | Hughes, AN. 1967. Chem Ind. 16: 662-3. PMID: 6046900
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Benzo[c]cinnoline, 1 g | sc-268552 | 1 g | $306.00 |