方案
98%
mp
74-77 °C (lit.)
官能团
thiocarbamate
SMILES字符串
CN1C(=O)Sc2ccccc12
InChI
1S/C8H7NOS/c1-9-6-4-2-3-5-7(6)11-8(9)10/h2-5H,1H3
InChI key
LSMMRJUHLKJNLR-UHFFFAOYSA-N
一般描述
3-Methyl-2(3H)-benzothiazolone is a five-membered heterocyclic compound. Its crystals belong to the orthorhombic crystal system and space group Pbca.
应用
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.
储存分类代码
13 - Non Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
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)
Original TDAE reactivity in benzoxa-and benzothiazolone series.
Nadji-Boukrouche AR, et al.
ARKIVOC (Gainesville, FL, United States), 10, 358-370 (2010)
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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