532-55-8
Chemical Structure
Benzoyl isothiocyanate
- CAS No.: 532-55-8
- Formula:C8H5NOS
- Molecular Weight:163.20
IUPAC Name: benzoyl isothiocyanate
InChIKey: CPEKAXYCDKETEN-UHFFFAOYSA-N
SMILES: O=C(N=C=S)C1=CC=CC=C1
Biological Activity: Benzoyl isothiocyanate is an aromatic isothiocyanate derivative with antibacterial and acaricidal activities. Benzoyl isothiocyanate inhibits the growth of specific oral bacteria, and also serves as an intermediate for the synthesis of heterocyclic compounds such as thiazolidine and quinazoline derivatives. Benzoyl isothiocyanate exhibits acaricidal activity against Dermatophagoides farina (dust mite) and D. pteronyssinus (house dust mite). Benzoyl isothiocyanate can be used in research related to bacterial infection, pest control and organic synthesis[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Benzoyl isothiocyanate | 99.79% | Benzoyl isothiocyanate is an aromatic isothiocyanate derivative with antibacterial and acaricidal activities. Benzoyl isothiocyanate inhibits the growth of specific oral bacteria, and also serves as an intermediate for the synthesis of heterocyclic compounds such as thiazolidine and quinazoline derivatives. Benzoyl isothiocyanate exhibits acaricidal activity against Dermatophagoides farina (dust mite) and D. pteronyssinus (house dust mite). Benzoyl isothiocyanate can be used in research related to bacterial infection, pest control and organic synthesis. | ||||||||||||||||||||
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References
- [1]. Douglass I B. Some Derivatives of Benzoyl and Furoyl Isothiocyanates and their Use in Synthesizing Heterocyclic Compounds. J Am Chem Soc, 1934, 56(3): 719-721.
- [2]. Kim MG, et al. Growth-inhibiting activities of phenethyl isothiocyanate and its derivatives against intestinal bacteria. Journal of food science. 2009 Oct;74(8):M467-71. [Content Brief]
- [3]. Kim H W, et al. Antibacterial activities of phenethyl isothiocyanate and its derivatives against human oral pathogens. J Korean Soc Appl Biol Chem, 2009, 52: 555-559.
