7066-67-3 Usage
Molecular structure
2-[2-(4-chlorophenyl)ethenyl]-5-[(3-phenoxyphenyl)methylidene][1,3]thiazolo[3,2-b][1,2,4]triazol-6(5H)-one has a complex molecular structure that includes a thiazole ring, a triazol-6(5H)-one moiety, phenyl and chlorophenyl groups.
Thiazole ring
The compound contains a five-membered heterocyclic ring, which consists of four carbon atoms and one nitrogen atom, with the nitrogen atom being part of the ring.
Triazol-6(5H)-one moiety
This moiety is a five-membered heterocyclic ring with three nitrogen atoms and two oxygen atoms, one of which is a hemiketal oxygen, giving the ring a 5H (five hydrogen) configuration.
Phenyl and chlorophenyl groups
The compound contains a phenyl group (a six-membered ring with alternating single and double carbon-carbon bonds) and a chlorophenyl group (a phenyl ring with one chlorine atom attached).
Potent enzyme inhibitor
The compound is a strong inhibitor of certain enzymes, which may have potential pharmacological applications.
Potential pharmacological applications
Due to its enzyme-inhibiting properties, the compound may have uses in medicine, but further research is needed to determine its specific applications.
Ongoing research
The precise properties and uses of 2-[2-(4-chlorophenyl)ethenyl]-5-[(3-phenoxyphenyl)methylidene][1,3]thiazolo[3,2-b][1,2,4]triazol-6(5H)-one are still under investigation, and more studies are required to fully understand its potential in medicine and chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 7066-67-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,6 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7066-67:
(6*7)+(5*0)+(4*6)+(3*6)+(2*6)+(1*7)=103
103 % 10 = 3
So 7066-67-3 is a valid CAS Registry Number.
7066-67-3Relevant academic research and scientific papers
Synthesis of bis(trifluoromethyl)phenylthallium and bis(trifluoromethyl)thallium acetate. Oxidative trifluoromethylation with bis(trifluoromethyl)thallium(III) compounds
Nair,Morrison
, p. 2816 - 2820 (2008/10/08)
The reaction of Cd(CF3)2·glyme with TlPhCl2 forms TlPh(CF3)2, which is isolated in 87% yield after 72 h. If TlPh(OAc)2 is the thallium source, TlPh(CF3)2 is generated in 2 h; however, the isolated yield is lower because acetate reacts with Cd(CF3)2·glyme, resulting in CH3COF. The interaction of Cd(CF3)2·glyme with Tl(OAc)3 produces Tl(CF3)2OAc, 46%, within 45 min. The possibility of utilizing (trifluoromethyl)thallium(III) species in oxidative trifluoromethylation reactions was screened by employing several classic low-valent metallic species as substrates. The reaction of elemental mercury was the most informative, yielding Hg(CF3)2 in 77% yield in glyme but generating a mixture of HgPh(CF3) and Hg(CF3)2 when CH2Cl2 was the solvent. These results are interpreted by postulating mercury insertion into the Tl-Ph bond, resulting in PhHgTl(CF3)2, which decomposes to generate HgPh(CF3). The formation of Hg(CF3)2 is attributed to the reaction of HgPh(CF3) with TlCF3.
