Molecular structure of Dibenzosuberone, CAS Number: 1210-35-1
Dibenzosuberone (CAS 1210-35-1)
Alternate Names:
Dibenzosuberan-5-one, Dibenzocycloheptenone
CAS Number:
1210-35-1
Purity:
≥97%
Molecular Weight:
208.26
Molecular Formula:
C15H12O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
Dibenzosuberone is a polycyclic aromatic hydrocarbon (PAH) that occurs naturally in the environment. It is generated during the combustion of organic substances and is present in coal tar and petroleum-based products. Furthermore, it serves as a component in the production of dyes, plastics, rubber, and various industrial goods. Research has been conducted to investigate its potential carcinogenic properties and its impact on the environment, making it a subject of interest in scientific studies.
Dibenzosuberone (CAS 1210-35-1) References
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- 2H NMR and X-ray diffraction studies of methyl rotation in crystals of ortho-methyldibenzocycloalkanones. | Cizmeciyan, D., et al. 2005. Solid State Nucl Magn Reson. 28: 1-8. PMID: 16026685
- Evidence for the involvement of the monoaminergic system in the antidepressant-like action of two 4-amine derivatives of 10,11-dihydro-5H-dibenzo [a,d] cycloheptane in mice evaluated in the tail suspension test. | Duarte, FS., et al. 2008. Prog Neuropsychopharmacol Biol Psychiatry. 32: 368-74. PMID: 17920179
- Synthesis of novel, potentially biologically active dibenzosuberone derivatives. | Merkas, S., et al. 2005. Molecules. 10: 1429-37. PMID: 18007539
- Sensitive extractive spectrophotometric methods for the determination of nortriptyline hydrochloride in pharmaceutical formulations. | Misiuk, W. and Tykocka, A. 2007. Chem Pharm Bull (Tokyo). 55: 1655-61. PMID: 18057736
- Design, synthesis, and biological evaluation of novel disubstituted dibenzosuberones as highly potent and selective inhibitors of p38 mitogen activated protein kinase. | Koeberle, SC., et al. 2012. J Med Chem. 55: 5868-77. PMID: 22676210
- Antiinflammatory and aldose reductase inhibitory activity of some tricyclic arylacetic acids. | Cerelli, MJ., et al. 1986. J Med Chem. 29: 2347-51. PMID: 3097317
- Azaacenodibenzosuberones. | Brosius, V., et al. 2020. J Org Chem. 85: 296-300. PMID: 31686519
- Synthesis of Dibenzosuberones Bearing an Isoxazole Group via Palladium-Catalyzed Intramolecular C-H/C-Br Bond Cross-Coupling of Ortho-Aroylated 3,5-Diarylisoxazoles. | Chao, T., et al. 2020. J Org Chem. 85: 5559-5569. PMID: 32212605
- Development and Validation of Stability Indicating High-Performance Liquid Chromatographic Method for Determination of Cyproheptadine Hydrochloride, its Impurity And Degradation Product. | Abdelrahman, MM., et al. 2021. J Chromatogr Sci. 59: 128-133. PMID: 33137815
- Simultaneous spectrophotometric determination of fluphenazine HCl and nortriptyline HCl in presence of their potential impurities perphenazine and dibenzosuberone in bulk and pharmaceutical formulation. | Magdy, MA., et al. 2022. Spectrochim Acta A Mol Biomol Spectrosc. 282: 121695. PMID: 35933777
- Stability of amitriptyline hydrochloride in a commercial aqueous solution. | Roman, R., et al. 1979. J Pharm Sci. 68: 1329-30. PMID: 512874
- Rapid high pressure liquid chromatographic determination of amitriptyline hydrochloride in tablets and injectables: collaborative study. | Walker, ST. 1983. J Assoc Off Anal Chem. 66: 1196-202. PMID: 6630133
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Dibenzosuberone, 25 g | sc-239683 | 25 g | $77.00 |