InChI
1S/C8H7NOS/c1-9-6-4-2-3-5-7(6)11-8(9)10/h2-5H,1H3
SMILES string
CN1C(=O)Sc2ccccc12
InChI key
LSMMRJUHLKJNLR-UHFFFAOYSA-N
assay
98%
mp
74-77 °C (lit.)
functional group
thiocarbamate
General description
3-Methyl-2(3H)-benzothiazolone is a five-membered heterocyclic compound. Its crystals belong to the orthorhombic crystal system and space group Pbca.
Application
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. It may be used for the synthesis of imidazole derivatives having 2(3H)-benzothiazolone moiety, which are potential antifungal agents.
存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Original TDAE reactivity in benzoxa-and benzothiazolone series.
Nadji-Boukrouche AR, et al.
ARKIVOC (Gainesville, FL, United States), 10, 358-370 (2010)
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
New imidazole derivatives of 2 (3H)-benzazolones as potential antifungal agents.
Petrov O, et al.
ChemInform, 40(31) (2009)
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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