1029-96-5 Usage
Description
2,6-Diphenyl-4H-thiopyran-4-one 96 is a chemical compound with a unique molecular structure that features a thiopyranone core and diphenyl substituents. 2 6-DIPHENYL-4H-THIOPYRAN-4-ONE 96 has attracted significant attention due to its potential applications in various fields, particularly in the pharmaceutical industry.
Uses
Used in Pharmaceutical Industry:
2,6-Diphenyl-4H-thiopyran-4-one 96 is used as a pharmacophore model for the development of novel inhibitors of ubiquitin isopeptidases. These inhibitors have the potential to induce p53-independent cell death, which can be beneficial in the treatment of various diseases, including cancer.
Used in Dye Industry:
2,6-Diphenyl-4H-thiopyran-4-one 96 can also be utilized as a component in the synthesis of dyes. Its unique chemical structure and properties make it a valuable candidate for creating dyes with specific characteristics, such as color intensity, stability, and solubility.
Used in Metabolite Research:
In addition to its applications in the pharmaceutical and dye industries, 2,6-diphenyl-4H-thiopyran-4-one 96 can be employed in metabolite research. Its chemical properties and interactions with other molecules make it a promising candidate for studying metabolic pathways and identifying potential biomarkers for various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 1029-96-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,2 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1029-96:
(6*1)+(5*0)+(4*2)+(3*9)+(2*9)+(1*6)=65
65 % 10 = 5
So 1029-96-5 is a valid CAS Registry Number.
InChI:InChI=1/C17H12OS/c18-15-11-16(13-7-3-1-4-8-13)19-17(12-15)14-9-5-2-6-10-14/h1-12H
1029-96-5Relevant articles and documents
-
Zupan
, p. 305,306,308 (1976)
-
Substituted sulfur aromatic heterocyclic compound, preparation method and application thereof
-
, (2020/11/23)
The present invention provides a sulfur aromatic heterocyclic compound represented by a formula I, and an optical isomer thereof, wherein Y is an anion, R1 is NR4R5, hydrogen, halogen, a C1-C4 alkyl group, a C1-C4 alkoxy group, a trifluoromethoxy group
The reaction of unsaturated carbonyl compounds with "activated" sulfur
Chiacchio, Ugo,Corsaro, Antonino,Rescifina, Antonio,Testa, Maria Gabriella,Purrello, Giovanni
, p. 223 - 229 (2007/10/02)
In a reinvestigation of the sulfuration reaction of cinnamylideneacetophenone (1) with sulfur and triethylamine at room temperature, new products 6-benzoyl-3-phenyl-1,2-dithiolo1,2-dithiole (5), 6-benzoyl-3-phenyl-1,2-dithiine (6) and 5-benzoyl-3-b
