86239-19-2 Usage
Uses
Used in Chemical Synthesis:
(3Z)-3-[(4-chlorophenyl)methylidene]-5-ethylthiophen-2(3H)-one is used as a building block in the chemical synthesis industry for the creation of other compounds. Its unique structure, which includes a chlorophenyl and an ethyl group attached to a thiophene ring, makes it a valuable component in developing new chemical entities.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (3Z)-3-[(4-chlorophenyl)methylidene]-5-ethylthiophen-2(3H)-one is used as a starting material for the development of new drugs. Its potential biological activity and therapeutic properties are of interest to researchers, who are investigating its possible applications in medicine. Further studies are necessary to determine its full potential in this field.
Used in Biological Activity Studies:
(3Z)-3-[(4-chlorophenyl)methylidene]-5-ethylthiophen-2(3H)-one is utilized in biological activity studies to explore its potential effects on various biological systems. (3Z)-3-[(4-chlorophenyl)methylidene]-5-ethylthiophen-2(3H)-one's structure and composition suggest it may interact with biological molecules, offering opportunities for new discoveries in the life sciences. Ongoing research aims to uncover its specific mechanisms of action and potential applications in therapeutics or other biological contexts.
Check Digit Verification of cas no
The CAS Registry Mumber 86239-19-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,2,3 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 86239-19:
(7*8)+(6*6)+(5*2)+(4*3)+(3*9)+(2*1)+(1*9)=152
152 % 10 = 2
So 86239-19-2 is a valid CAS Registry Number.
86239-19-2Relevant academic research and scientific papers
Benzylidene-Thiolactone Rearrangement: Synthesis and Rearrangement of 5-Substituted 3-Benzylidene-4-thiolen-2-ones
Heindel, Ned D.,Conley, Richard A.,Minatelli, John A.,Boschelli, Diane Harris
, p. 3051 - 3053 (2007/10/02)
Condensation of 5-substituted 4-thiolen-2-ones (1) with aromatic aldehydes (2) in anhydrous ethanolic HCl generates the 3-benzylidene derivatives 3.These can be rearranged in base (benzylidene-thiolactone rearrangement) to 2,5-disubstituted thiophene-3-carboxylic acids (4, 5, or 6).
