57334-18-6 Usage
Structure
A derivative of benzothiazolone with a methyl group at the 3-position and a nitro group at the 6-position.
Versatility
Serves as a building block in organic synthesis.
Applications
Used in the development of pharmaceuticals, dyes, and other specialty chemicals.
Biological activities
Studied for potential applications in medicine and agriculture.
Importance
Has significant industrial and scientific applications due to its unique chemical structure and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 57334-18-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,3,3 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 57334-18:
(7*5)+(6*7)+(5*3)+(4*3)+(3*4)+(2*1)+(1*8)=126
126 % 10 = 6
So 57334-18-6 is a valid CAS Registry Number.
57334-18-6Relevant academic research and scientific papers
The reaction of 3-methylthiazolium derivatives with superoxide
Itoh, Takashi,Nagata, Kazuhiro,Okada, Mamiko,Ohsawa, Akio
, p. 4859 - 4870 (2007/10/02)
3-Methylbenzothiazolium salts were allowed to react with superoxide to afford dimeric bis[o-(N-formyl-N-methylamino)phenyl]disulfides and 3-methyl-2-benzothiazolones. The reaction was applied to monocyclic thiazolium salts, and novel ten-membered ring com
THE REACTION OF 3-METHYLBENZOTHIAZOLIUM SALTS WITH SUPEROXIDE
Itoh, Takashi,Nagata, Kazuhiro,Okada, Mamiko,Ohsawa, Akio
, p. 361 - 362 (2007/10/02)
3-Methylbenzothiazolium salts reacted with superoxide to afford dimeric bisdisulfides and 3-methyl-2-benzothiazolones.The reaction was entirely specific for superoxides, and is of interest from the biological and mechanis
