102565-09-3 Usage
Description
(2E)-2-(hydroxy[(E)-2-phenyl-2-thiophen-2-ylethenyl]aminomethylidene)-5-(trifluoromethyl)-1-benzothiophen-3(2H)-one is a complex organic molecule with a benzothiophene core, a trifluoromethyl group, and a hydroxy functionality. It also features a substituted amino group and a double bond, giving it a distinct structure. (2E)-2-(hydroxy[(E)-2-phenyl-2-thiophen-2-ylethenyl]aminomethylidene)-5-(trifluoromethyl)-1-benzothiophen-3(2H)-one may have potential applications in medicinal chemistry or materials science due to its unique combination of functional groups and stereochemistry.
Uses
Used in Medicinal Chemistry:
(2E)-2-(hydroxy[(E)-2-phenyl-2-thiophen-2-ylethenyl]aminomethylidene)-5-(trifluoromethyl)-1-benzothiophen-3(2H)-one is used as a potential pharmaceutical candidate for the development of new drugs. Its unique structure and functional groups may allow for the modulation of biological targets and pathways, leading to the discovery of novel therapeutic agents.
Used in Materials Science:
(2E)-2-(hydroxy[(E)-2-phenyl-2-thiophen-2-ylethenyl]aminomethylidene)-5-(trifluoromethyl)-1-benzothiophen-3(2H)-one is used as a building block for the synthesis of new materials with specific properties. Its combination of functional groups and stereochemistry may contribute to the development of advanced materials with applications in various industries, such as electronics, coatings, or polymers.
However, it is important to note that further research and characterization would be necessary to fully understand the properties and potential uses of this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 102565-09-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,5,6 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 102565-09:
(8*1)+(7*0)+(6*2)+(5*5)+(4*6)+(3*5)+(2*0)+(1*9)=93
93 % 10 = 3
So 102565-09-3 is a valid CAS Registry Number.
102565-09-3Relevant articles and documents
Stereoselective disposition of the geometric isomers of a novel lipoxygenase cyclo-oxygenase inhibitor in dog and photochemical interconversion of its isomers
Matuszewski,Kanovsky,Constanzer,Yeh,Bayne
, p. 880 - 884 (1988)
A sensitive (10 ng/mL) and specific high-performance liquid chromatographic (HPLC) assay, with electrochemical (EC) detection, for the geometric isomers of 3-hydroxy-N-(2-phenyl-2-(2-thienyl)ethenyl-5-(trifluoromethyl)benzo(b thiophene-2-carboxamide in dog and human plasma has been developed. Both isomers strongly absorb light, leading to an efficient E ? Z photoisomerization. After iv administration of a single isomer (Z) to a dog, only the Z isomer was detected in plasma; no in vivo conversion to the E isomer was observed. However, when a mixture of the E and Z isomers (58.6:41.4) was administered in the same manner to the same dog, the E:Z ratio decreased significantly to 47.5:52.5 six hours after drug administration, indicating stereoselective disposition of the isomers. The elimination of the E isomer was found to be faster than that of the Z isomer.
N-alkenyl-3-hydroxybenzo[b]thiophene-2-carboxamide derivatives as dual cyclooxygenase and lipoxygenase inhibitors
-
, (2008/06/13)
N-Alkenyl-3-hydroxybenzo[b]thiophene-2-carboxamide derivatives have been prepared by: (1) treating a substituted 2-halobenzoate with thioacetamide followed by N-alkenylation with appropriate agents, such as aldehydes, ketones, enol ethers, epoxides, aceta
