1198437-98-7 Usage
Molecular Structure
1H-Indazole, 6-bromo-3-fluoro-4-nitro-1-(phenylsulfonyl)is a complex organic compound with an indazole ring structure, featuring a bromine atom at the 6th position, a fluorine atom at the 3rd position, a nitro group at the 4th position, and a phenylsulfonyl group at the 1st position.
Functional Groups
The compound has several distinct functional groups, including a bromine atom, a fluorine atom, a nitro group, and a phenylsulfonyl group, which contribute to its chemical reactivity and potential applications.
Reactivity
Due to its diverse chemical structure, 1H-Indazole, 6-bromo-3-fluoro-4-nitro-1-(phenylsulfonyl)may be highly reactive, allowing it to interact with various biological systems.
Potential Applications
This compound may have potential applications in pharmaceutical research and development, as its complex structure could make it suitable for various therapeutic uses.
Further Evaluation
The specific properties and potential uses of 1H-Indazole, 6-bromo-3-fluoro-4-nitro-1-(phenylsulfonyl)would need to be further evaluated through thorough scientific studies to determine its suitability for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1198437-98-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,8,4,3 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1198437-98:
(9*1)+(8*1)+(7*9)+(6*8)+(5*4)+(4*3)+(3*7)+(2*9)+(1*8)=207
207 % 10 = 7
So 1198437-98-7 is a valid CAS Registry Number.
1198437-98-7Relevant articles and documents
Indazole derivatives for use in the treatment of influenza virus infection
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, (2016/06/01)
The present invention is directed to compounds for use in the treatment or prevention of influenza virus infection.
BENZPYRAZOLE DERIVATIVES AS INHIBITORS OF P13 KINASES
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, (2011/06/25)
The invention is directed to certain novel compounds. Specifically, the invention is directed to compounds of formula (I) and salts thereof. The compounds of the invention are inhibitors of PI3-kinase activity.
