460281
3-Methyl-2(3H)-benzothiazolone
98%
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About This Item
Formula empirica (notazione di Hill):
C8H7NOS
Numero CAS:
Peso molecolare:
165.21
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Saggio
98%
Punto di fusione
74-77 °C (lit.)
Gruppo funzionale
thiocarbamate
Stringa SMILE
CN1C(=O)Sc2ccccc12
InChI
1S/C8H7NOS/c1-9-6-4-2-3-5-7(6)11-8(9)10/h2-5H,1H3
LSMMRJUHLKJNLR-UHFFFAOYSA-N
Descrizione generale
3-Methyl-2(3H)-benzothiazolone is a five-membered heterocyclic compound. Its crystals belong to the orthorhombic crystal system and space group Pbca.[1]
Applicazioni
3-Methyl-2(3H)-benzothiazolone may be used for the synthesis of 2,3-dihydro-3-methyl-2- oxobenzo[d]oxazole-6-carbaldehyde and the 2,3-dihydro-3-methyl-2-oxobenzo[d]thiazole-6-carbaldehyde.[2] It may be used for the synthesis of imidazole derivatives having 2(3H)-benzothiazolone moiety, which are potential antifungal agents.[3]
Codice della classe di stoccaggio
13 - Non Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
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Original TDAE reactivity in benzoxa-and benzothiazolone series.
Nadji-Boukrouche AR, et al.
ARKIVOC (Gainesville, FL, United States), 10, 358-370 (2010)
New imidazole derivatives of 2 (3H)-benzazolones as potential antifungal agents.
Petrov O, et al.
ChemInform, 40(31) (2009)
A El-Brashy et al.
International journal of biomedical science : IJBS, 2(4), 406-413 (2006-12-01)
A simple and sensitive kinetic method is described for the determination of ketoprofen in pure form, pharmaceuticals and biological fluids. The method utilizes an oxidative- coupling reaction based upon oxidation of 3-methyl-2-benzo-thiazolinone hydrazone hydrochloride (MBTH) with Ce(IV) in presence of
3-Methyl-2 (3H)-benzothiazolone, C8H7NOS.
Rudd S and Barany G.
Acta Crystallographica Section C, Structural Chemistry, 40(12), 2118-2120 (1984)
María D Santi et al.
Bioorganic & medicinal chemistry, 27(16), 3722-3728 (2019-07-06)
The lack of secure therapies for hyperpigmentation disorders, without serious adverse effects, and the latest reports relating melanogenic disorders with development of neurodegenerative diseases, encourage the continuing search for new drugs for the treatment of such disorders. In this sense
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