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Molecular structure of Indolo[3,2-b]carbazole, CAS Number: 6336-32-9
Indolo[3,2-b]carbazole (CAS 6336-32-9)
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Application:
Indolo[3,2-b]carbazole is a useful biochemical for proteomics research
CAS Number:
6336-32-9
Purity:
≥97%
Molecular Weight:
256.31
Molecular Formula:
C18H12N2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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Indolo[3,2-b]carbazole is a useful biochemical for proteomics research. Indolo[3,2-b]carbazole, an aromatic heterocyclic compound, has garnered attention for its applications in medicinal chemistry, photochemistry, and biochemistry. In photochemistry, it has been investigated as a photosensitizer capable of generating singlet oxygen. As for biochemistry, this compound has been the subject of studies exploring its potential as a reagent for synthesizing diverse bioactive compounds, including peptides and nucleotides.
Indolo[3,2-b]carbazole (CAS 6336-32-9) References
- Facile synthesis of novel indolo[3,2-b]carbazole derivatives and a chromogenic-sensing 5,12-dihydroindolo[3,2-b]carbazole. | Gu, R., et al. 2008. Org Biomol Chem. 6: 2484-7. PMID: 18600267
- Synthesis of indolo[3,2-b]carbazole-based new colorimetric receptor for anions: A unique color change for fluoride ions. | Mahapatra, AK., et al. 2010. Beilstein J Org Chem. 6: 12. PMID: 20485594
- Synthesis and properties of methoxyphenyl-substituted derivatives of indolo[3,2-b]carbazole. | Simokaitiene, J., et al. 2012. J Org Chem. 77: 4924-31. PMID: 22537513
- Indolocarbazole-based ligands for ladder-type four-coordinate boron complexes. | Curiel, D., et al. 2012. Org Lett. 14: 3360-3. PMID: 22716949
- Improved Spectral Coverage and Fluorescence Quenching in Donor-acceptor Systems Involving Indolo[3-2-b]carbazole and Boron-dipyrromethene or Diketopyrrolopyrrole. | Khetubol, A., et al. 2015. Photochem Photobiol. 91: 637-53. PMID: 25683093
- The Brassica-derived phytochemical indolo[3,2-b]carbazole protects against oxidative DNA damage by aryl hydrocarbon receptor activation. | Faust, D., et al. 2017. Arch Toxicol. 91: 967-982. PMID: 26856715
- Efficient organic dyes based on perpendicular 6,12-diphenyl substituted indolo[3,2-b]carbazole donor. | Xiao, Z., et al. 2016. Photochem Photobiol Sci. 15: 1514-1523. PMID: 27830860
- Synthesis of Indolo[3,2- b]carbazole-Based Boron Complexes with Tunable Photophysical and Electrochemical Properties. | Mula, S., et al. 2018. J Org Chem. 83: 14406-14418. PMID: 30387347
- Antifungal activity of selected Malassezia indolic compounds detected in culture. | Gaitanis, G., et al. 2019. Mycoses. 62: 597-603. PMID: 30636018
- Design and Characterization of New D-A Type Electrochromic Conjugated Copolymers Based on Indolo[3,2-b]Carbazole, Isoindigo and Thiophene Units. | Zhang, Y., et al. 2019. Polymers (Basel). 11: PMID: 31597368
- A Biomimetic, One-Step Transformation of Simple Indolic Compounds to Malassezia-Related Alkaloids with High AhR Potency and Efficacy. | Mexia, N., et al. 2019. Chem Res Toxicol. 32: 2238-2249. PMID: 31647221
- Revisiting Indolo[3,2-b]carbazole: Synthesis, Structures, Properties, and Applications. | Zhao, M., et al. 2020. Angew Chem Int Ed Engl. 59: 9678-9683. PMID: 32162418
- Novel Red Light-Absorbing Organic Dyes Based on Indolo[3,2-b]carbazole as the Donor Applied in Co-Sensitizer-Free Dye-Sensitized Solar Cells. | Xiao, Z., et al. 2021. Materials (Basel). 14: PMID: 33807483
- Synthesis and characterization of novel donor-acceptor type neutral green electrochromic polymers containing an indolo[3,2-b]carbazole donor and diketopyrrolopyrrole acceptor. | Zhang, Y., et al. 2018. RSC Adv. 8: 21252-21264. PMID: 35539948
- Eight Indole Alkaloids from the Roots of Maerua siamensis and Their Nitric Oxide Inhibitory Effects. | Nukulkit, S., et al. 2022. Molecules. 27: PMID: 36364385
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Arnt 1.Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Indolo[3,2-b]carbazole, 10 mg | sc-311367 | 10 mg | $686.00 | |||
Indolo[3,2-b]carbazole, 100 mg | sc-311367A | 100 mg | $1840.00 |