883001-24-9 Usage
General Description
7-Bromo-5-fluoro-3-methyl-1H-indole is a chemical compound with the molecular formula C9H7BrFN. It is a heterocyclic aromatic compound that contains a five-membered ring with three carbon atoms, one nitrogen atom, and one bromine atom. The compound also contains a fluorine substituent and a methyl group. 7-Bromo-5-fluoro-3-methyl-1H-indole is used in organic synthesis and pharmaceutical research, and it has potential applications in the development of new drugs and materials. It is important to handle this compound with caution, as it may have hazardous properties and should be used in a controlled laboratory environment.
Check Digit Verification of cas no
The CAS Registry Mumber 883001-24-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,3,0,0 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 883001-24:
(8*8)+(7*8)+(6*3)+(5*0)+(4*0)+(3*1)+(2*2)+(1*4)=149
149 % 10 = 9
So 883001-24-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H7BrFN/c1-5-4-12-9-7(5)2-6(11)3-8(9)10/h2-4,12H,1H3
883001-24-9Relevant articles and documents
QUINOXALINE DERIVATIVES
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Page/Page column 27, (2021/07/24)
The present invention relates to compounds according to general formula (I), which act as modulators of the glucocorticoid receptor and can be used in the treatment and/or prophylaxis of disorders which are at least partially mediated by the glucocorticoid receptor.
SUBSTITUTED TRIAZOLO QUINOXALINE DERIVATIVES
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Page/Page column 44, (2020/02/14)
The present invention relates to compounds according to general formula (I) which act as modulators of the glucocorticoid receptor and can be used in the treatment and/or prophylaxis of disorders which are at least partially mediated by the glucocorticoid receptor.
PROCESS FOR PREPARING 7-(ACRYLOYL)INDOLES
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Page/Page column 8-9, (2008/06/13)
The present invention involves a process for preparing substituted indoles, such as DTSI involving two sequential cross-coupling reactions.
