4337-47-7 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
6-methyl-1,2-benzothiazol-3(2H)-one is used as a building block in the synthesis of pharmaceuticals and agrochemicals for its versatile chemical properties and potential therapeutic effects.
Used in Antimicrobial Applications:
6-methyl-1,2-benzothiazol-3(2H)-one is used as an antimicrobial agent for its ability to inhibit the growth of various microorganisms, making it a valuable component in the development of new antimicrobial drugs and treatments.
Used in Antifungal Applications:
6-methyl-1,2-benzothiazol-3(2H)-one is used as an antifungal agent for its effectiveness in combating fungal infections, offering potential in the creation of new antifungal medications and therapies.
Used in Antioxidant Applications:
6-methyl-1,2-benzothiazol-3(2H)-one is used as an antioxidant for its ability to neutralize harmful free radicals, which can protect cells from oxidative damage and contribute to the development of health-promoting compounds.
Used in Fluorescent Dyes and Chemical Sensors:
6-methyl-1,2-benzothiazol-3(2H)-one is used in the development of fluorescent dyes and chemical sensors for its unique optical and electronic properties, which can be harnessed for various analytical and diagnostic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 4337-47-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,3 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4337-47:
(6*4)+(5*3)+(4*3)+(3*7)+(2*4)+(1*7)=87
87 % 10 = 7
So 4337-47-7 is a valid CAS Registry Number.
4337-47-7Relevant academic research and scientific papers
NEUROPROTECTIVE PDI MODULATING SMALL MOLECULES AND METHODS OF USE THEREOF
-
, (2020/06/19)
The present disclosure provides, inter alia, compounds and compositions having the formula (I) as defined herein. Methods of using and making such compounds and compositions are also provided. The present disclosure further provides screening methods, including detectable probes as well as diagnostic methods and methods for monitoring the progress of a disease, such as a neurodegenerative disease.
An efficient approach to construct benzisothiazol-3(2: H)-ones via copper-catalyzed consecutive reaction of 2-halobenzamides and carbon disulfide
Li, Ting,Yang, Lei,Ni, Kaidong,Shi, Zhenyu,Li, Fei,Chen, Dongyin
, p. 6297 - 6303 (2016/07/11)
An efficient copper-catalyzed reaction for the synthesis of benzisothiazol-3(2H)-ones has been developed, starting from easily available 2-halobenzamides and carbon disulfide, which gave the corresponding target products in 30-89% yield for 25 examples. The reaction proceeds via a consecutive process with S-C bond and S-N bond formation.
Concise approach to benzisothiazol-3(2 H)-one via copper-catalyzed tandem reaction of o -bromobenzamide and potassium thiocyanate in water
Wang, Fei,Chen, Chao,Deng, Geng,Xi, Chanjuan
experimental part, p. 4148 - 4151 (2012/06/18)
A concise approach to various benzisothiazol-3(2H)-one derivatives has been developed by copper-catalyzed the reaction of o-bromobenzamide derivatives with potassium thiocyanate (KSCN) in water. The reaction proceeds via a tandem reaction with S-C bond and S-N bond formation.
