1097802-78-2 Usage
General Description
6,7-Difluoro-2,3-dihydro-4H-1-benzothiopyran-4-one is a chemical compound with a complex molecular structure. It belongs to the class of organofluorine compounds, which are organic compounds that contain fluorine. 6,7-Difluoro-2,3-dihydro-4H-1-benzothiopyran-4-one also consists of a benzothiopyran, a type of chemical formula characterized by a fused ring system consisting of a benzene ring and thiopyran. Benzothiopyrans are widely used in the field of medicinal chemistry due to their biological activity. The specific properties, behaviors, and reactivity of 6,7-Difluoro-2,3-dihydro-4H-1-benzothiopyran-4-one would need to be further explored through detailed scientific research and experimentation.
Check Digit Verification of cas no
The CAS Registry Mumber 1097802-78-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,7,8,0 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1097802-78:
(9*1)+(8*0)+(7*9)+(6*7)+(5*8)+(4*0)+(3*2)+(2*7)+(1*8)=182
182 % 10 = 2
So 1097802-78-2 is a valid CAS Registry Number.
1097802-78-2Relevant articles and documents
SUBSTITUTED SULFONE-CONTAINING TRICYCLIC COMPOUNDS AND USES THEREOF
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Page/Page column 30, (2014/05/24)
The present invention relates to substituted sulfone-containing tricyclic compounds and analogues thereof which inhibit Bak-mediated apoptosis. The invention further relates to pharmaceutical compositions comprising a compound of the present invention and to methods of inhibiting a Bak-mediated apoptotic pathway and Bak-mediated apoptosis in a cell.
Synthesis and biochemical evaluation of thiochromanone thiosemicarbazone analogues as inhibitors of cathepsin L
Song, Jiangli,Jones, Lindsay M.,Kumar, G. D. Kishore,Conner, Elizabeth S.,Bayeh, Liela,Chavarria, Gustavo E.,Charlton-Sevcik, Amanda K.,Chen, Shen-En,Chaplin, David J.,Trawick, Mary Lynn,Pinney, Kevin G.
, p. 450 - 453 (2012/09/25)
A series of 36 thiosemicarbazone analogues containing the thiochromanone molecular scaffold functionalized primarily at the C-6 position were prepared by chemical synthesis and evaluated as inhibitors of cathepsins L and B. The most promising inhibitors f
