73499-29-3 Usage
Uses
Used in Pharmaceutical Industry:
2,6-dimethyl-3,5-diphenyl-4H-pyran-4-thione is used as a potential therapeutic agent for its antioxidant and anti-inflammatory properties, which may contribute to the treatment of various diseases and conditions.
Used in Enzyme Inhibition:
2,6-dimethyl-3,5-diphenyl-4H-pyran-4-thione is used as an enzyme inhibitor, targeting various enzymes that play a role in disease progression. Its inhibitory effects on enzymes may contribute to the development of new drugs for treating specific conditions.
Used in Cancer Research:
2,6-dimethyl-3,5-diphenyl-4H-pyran-4-thione is used as a potential anti-cancer agent, as it has shown promising results in suppressing the growth of cancer cells. Further research is being conducted to explore its potential as a chemotherapeutic agent or in combination with existing treatments to enhance their efficacy.
Used in Drug Development:
2,6-dimethyl-3,5-diphenyl-4H-pyran-4-thione is used in the development of new drugs, as its unique structure and properties may offer novel therapeutic approaches for various medical conditions. Ongoing research aims to optimize its potential and explore its applications in medicine and industry.
Check Digit Verification of cas no
The CAS Registry Mumber 73499-29-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,4,9 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 73499-29:
(7*7)+(6*3)+(5*4)+(4*9)+(3*9)+(2*2)+(1*9)=163
163 % 10 = 3
So 73499-29-3 is a valid CAS Registry Number.
73499-29-3Relevant academic research and scientific papers
The Formation of Two Kinds of Thiophene Derivatives by the Reaction of the 4H-pyran-4-thione Derivative with Dimethyloxosulfonium Methylide in a One-pot Process
Yamaoka, Hiroshi,Mishima, Ikuhiro,Hanafusa, Terukiyo
, p. 1763 - 1764 (2007/10/02)
The reaction of 2,6-dimethyl-3,5-diphenyl-4H-pyran-4-thione with dimethyloxosulfonium methylide occurred facilely to give two kinds of 2-thienylacetones, accompanied by a five-membered α,β-unsaturated thione, a naphthothiophene derivative, and a hemithioacetal.
