Benzothiazole
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| Names | |||
|---|---|---|---|
| IUPAC name
1,3-Benzothiazole | |||
| Identifiers | |||
95-16-9  | |||
| ChEBI | CHEBI:45993 | ||
| ChEMBL | ChEMBL510309 | ||
| ChemSpider | 6952 | ||
| Jmol interactive 3D | Image | ||
| PubChem | 7222 | ||
| UNII | G5BW2593EP | ||
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| Properties | |||
| C7H5NS | |||
| Molar mass | 135.1863 g/mol | ||
| Density | 1.238 g/mL | ||
| Melting point | 2 °C (36 °F; 275 K) | ||
| Boiling point | 227 to 228 °C (441 to 442 °F; 500 to 501 K) | ||
| Supplementary data page | |||
| Refractive index (n), Dielectric constant (εr), etc. | |||
| Thermodynamic data |
Phase behaviour solid–liquid–gas | ||
| UV, IR, NMR, MS | |||
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| Infobox references | |||
Benzothiazole is an aromatic heterocyclic compound with the chemical formula C
7H
5NS. It is colorless, slightly viscous liquid. Although the parent compound, benzothiazole is not widely used, many of its derivatives are found in commercial products or in nature. A derivative of benzothiazole is the light-emitting component of luciferin, found in fireflies.
Structure and preparation
Benzothiazoles consist of a 5-membered 1,3-thiazole ring fused to a benzene ring. The nine atoms of the bicycle and the attached substituents are coplanar.
Benzothiazole are prepared by treatment of 2-mercaptoaniline with acid chlorides:[1]
- C6H4(NH2)SH + RC(O)Cl → C6H4(NH)SCR + HCl + H2O
Uses
This heterocyclic scaffold is readily substituted at the unique methyne centre in the thiazole ring. It is a thermally stable electron-withdrawing moiety with numerous applications in dyes such as thioflavin. Some drugs contain this group, examples being riluzole and pramipexole. The heterocycle is found in nature.[2] Accelerators for the vulcanization of rubber are based on 2-mercaptobenzothiazole.[3] This ring is a potential component in nonlinear optics (NLO).[4]
See also
- Benzothiazoles are related to thiazoles, which lack the fused benzene ring.
- Benzoxazoles, which substitute an oxygen for the sulfur atom.
References
- ↑ T. E. Gilchrist "Heterocyclic Chemistry" 3rd Edition, Longman, 1992.
- ↑ Lucille Le Bozec, Christopher J. Moody "Naturally Occurring Nitrogen–Sulfur Compounds. The Benzothiazole Alkaloids" Australian Journal of Chemistry 62(7) 639–647.doi:10.1071/CH09126
- ↑ Hans-Wilhelm Engels, Herrmann-Josef Weidenhaupt, Manfred Pieroth, Werner Hofmann, Karl-Hans Menting, Thomas Mergenhagen, Ralf Schmoll, Stefan Uhrlandt "Rubber, 4. Chemicals and Additives" in Ullmann's Encyclopedia of Industrial Chemistry 2004, Wiley-VCH, Weinheim. doi:10.1002/14356007.a23_365.pub2
- ↑ Hrobarik, P.; Sigmundova, I.; Zahradnik, P.; Kasak, P.; Arion, V.; Franz, E.; Clays, K. (2010). "Molecular Engineering of Benzothiazolium Salts with Large Quadratic Hyperpolarizabilities: Can Auxiliary Electron-Withdrawing Groups Enhance Nonlinear Optical Responses?". Journal of Physical Chemistry C 114 (50): 22289–22302. doi:10.1021/jp108623d.