289031-45-4 Usage
Description
(Z)-6,7-dihydro-2-p-tolyl-5H-1,4-dithiepine is a chemical compound belonging to the dithiepine class, which are heterocyclic compounds characterized by the presence of two sulfur atoms in their ring structure. This particular compound features a (Z) stereochemistry, indicating that the two substituents on the double bond are positioned on the same side of the ring. Additionally, it contains a p-tolyl group, which is a derivative of toluene with a methyl and a phenyl group attached. Dithiepines, in general, have been investigated for their potential biological activities, such as anti-cancer and anti-inflammatory properties. The specific characteristics and applications of (Z)-6,7-dihydro-2-p-tolyl-5H-1,4-dithiepine are subject to further research and depend on its individual properties.
Uses
Used in Pharmaceutical Industry:
(Z)-6,7-dihydro-2-p-tolyl-5H-1,4-dithiepine is used as a potential therapeutic agent for its possible anti-cancer and anti-inflammatory properties. (Z)-6,7-dihydro-2-p-tolyl-5H-1,4-dithiepine's unique structure and chemical properties make it a candidate for further research and development in the pharmaceutical sector, with the aim of creating novel treatments for various diseases.
Used in Chemical Research:
In the field of chemical research, (Z)-6,7-dihydro-2-p-tolyl-5H-1,4-dithiepine serves as a subject for studying the structure-activity relationship of dithiepine compounds. Understanding how its specific features contribute to its biological activities can provide valuable insights into the design and synthesis of new compounds with improved or novel therapeutic effects.
Used in Material Science:
(Z)-6,7-dihydro-2-p-tolyl-5H-1,4-dithiepine may also find applications in material science, particularly in the development of new materials with unique properties. The presence of sulfur atoms and the (Z) stereochemistry in the dithiepine ring structure could potentially influence the compound's reactivity, stability, and interaction with other molecules, making it an interesting candidate for further exploration in this field.
Check Digit Verification of cas no
The CAS Registry Mumber 289031-45-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,9,0,3 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 289031-45:
(8*2)+(7*8)+(6*9)+(5*0)+(4*3)+(3*1)+(2*4)+(1*5)=154
154 % 10 = 4
So 289031-45-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H14S2/c1-10-3-5-11(6-4-10)12-9-13-7-2-8-14-12/h3-6,9H,2,7-8H2,1H3
289031-45-4Relevant articles and documents
2,3-Dihydro-dithiin and -dithiepine-1,1,4,4-tetroxides: Small molecule non-peptide antagonists of the human galanin hGAL-1 receptor
Scott, Malcolm K.,Ross, Tina M.,Lee, Daniel H. S.,Wang, Hoau-Yan,Shank, Richard P.,Wild, Kenneth D.,Davis, Coralie B.,Crooke, Jeffrey J.,Potocki, Alexander C.,Reitz, Allen B.
, p. 1383 - 1391 (2007/10/03)
The neuropeptide galanin modulates several physiological functions such as cognition, learning, feeding behavior, and depression, probably via the galanin 1 receptor (GAL-R1). Using an HTS assay based on 125I-human galanin binding to the human
