397845-03-3 Usage
General Description
4-BROMO-2-METHYLTHIOBENZAMIDE is a chemical compound with the molecular formula C8H8BrNO2S. It is a white to off-white solid that is used primarily as an intermediate in the synthesis of pharmaceuticals and organic compounds. It is also used as a building block in the production of agrochemicals and other specialty chemicals. 4-BROMO-2-METHYLTHIOBENZAMIDE is a versatile compound that has applications in various industries, including agriculture, pharmaceuticals, and materials science. As with any chemical, proper safety precautions should be taken when handling and storing 4-BROMO-2-METHYLTHIOBENZAMIDE to ensure the safety of workers and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 397845-03-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,7,8,4 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 397845-03:
(8*3)+(7*9)+(6*7)+(5*8)+(4*4)+(3*5)+(2*0)+(1*3)=203
203 % 10 = 3
So 397845-03-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H8BrNS/c1-5-4-6(9)2-3-7(5)8(10)11/h2-4H,1H3,(H2,10,11)
397845-03-3Relevant articles and documents
Optimizing thiadiazole analogues of resveratrol versus three chemopreventive targets
Mayhoub, Abdelrahman S.,Marler, Laura,Kondratyuk, Tamara P.,Park, Eun-Jung,Pezzuto, John M.,Cushman, Mark
experimental part, p. 510 - 520 (2012/03/10)
Chemoprevention is an approach to decrease cancer morbidity and mortality through inhibition of carcinogenesis and prevention of disease progression. Although the trans stilbene derivative resveratrol has chemopreventive properties, its action is compromised by weak non-specific effects on many biological targets. Replacement of the stilbene ethylenic bridge of resveratrol with a 1,2,4-thiadiazole heterocycle and modification of the substituents on the two aromatic rings afforded potential chemopreventive agents with enhanced potencies and selectivities when evaluated as inhibitors of aromatase and NF-κB and inducers of quinone reductase 1 (QR1).
NOVEL HERBICIDES
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Page/Page column 78-79, (2009/04/25)
Compounds of formula (I) wherein the substituents are as defined in claim 1, are suitable for use as herbicides.
