871110-10-0 Usage
Indazole family
benzo[g]indazole core
A group of chemical compounds with a specific core structure, in this case, the benzo[g]indazole core, which is a fused ring system containing indazole.
Fluorophenyl group
4-fluorophenyl
A phenyl group (a six-membered aromatic ring with a hydrogen atom replaced by a fluorine atom) with a fluorine atom at the 4-position (the meta position).
Methylthio group
3-methylthio
A methyl group (a carbon atom with three hydrogen atoms) bonded to a sulfur atom, which in turn is connected to the benzo[g]indazole core.
Industrial applications
pharmaceutical research and development
The compound may have potential uses in the pharmaceutical industry, such as in the development of new drugs or the improvement of existing ones.
Further investigation
experimental studies and testing
To determine the specific properties and potential uses of 2-(4-fluorophenyl)-3-methylthio-4,5-dihydro-2H-benzo[g]indazole, additional research and testing through experimental studies would be required.
Check Digit Verification of cas no
The CAS Registry Mumber 871110-10-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,1,1 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 871110-10:
(8*8)+(7*7)+(6*1)+(5*1)+(4*1)+(3*0)+(2*1)+(1*0)=130
130 % 10 = 0
So 871110-10-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H15FN2S/c1-22-18-16-11-6-12-4-2-3-5-15(12)17(16)20-21(18)14-9-7-13(19)8-10-14/h2-5,7-10H,6,11H2,1H3
871110-10-0Relevant articles and documents
Regioselective synthesis of 1-aryl-3,4-substituted/annulated-5-(methylthio) pyrazoles and 1-aryl-3-(methylthio)-4,5-substituted/annulated pyrazoles
Peruncheralathan,Khan,Ila,Junjappa
, p. 10030 - 10035 (2007/10/03)
Highly efficient and regioselective synthesis of 1-aryl-3,4-substituted/ annulated-5-(methylthio)-pyrazoles and 1-aryl-3-(methylthio)-4,5-substituted/ annulated pyrazoles has been reported via cyclocondensation of arylhydrazines with either α-oxoketene dithioacetals or β-oxodithioesters.
