2080-41-3 Usage
Description
(Z)-3-[(Z)-3-oxo-1,3-diphenyl-prop-1-enyl]disulfanyl-1,3-diphenyl-prop-2-en-1-one is a complex organic molecule characterized by a long, unbranched carbon chain with two benzene rings and a disulfide (S-S) bond. It also features a ketone group, which is a carbon atom double-bonded to an oxygen atom, and the molecule is organized in a Z configuration, with substituent groups on the same side of the carbon-carbon double bond. This unique structure and reactivity may offer potential applications in various fields, such as pharmaceuticals, materials science, and organic synthesis.
Uses
Used in Pharmaceutical Applications:
(Z)-3-[(Z)-3-oxo-1,3-diphenyl-prop-1-enyl]disulfanyl-1,3-diphenyl-prop-2-en-1-one is used as a potential active pharmaceutical ingredient for [application reason] due to its unique molecular structure and reactivity.
Used in Materials Science:
In the field of materials science, (Z)-3-[(Z)-3-oxo-1,3-diphenyl-prop-1-enyl]disulfanyl-1,3-diphenyl-prop-2-en-1-one is used as a component in the development of novel materials for [application reason], leveraging its specific chemical properties.
Used in Organic Synthesis:
(Z)-3-[(Z)-3-oxo-1,3-diphenyl-prop-1-enyl]disulfanyl-1,3-diphenyl-prop-2-en-1-one serves as a key intermediate in organic synthesis for the production of various complex organic compounds for [application reason], taking advantage of its unique structural features and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 2080-41-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,8 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2080-41:
(6*2)+(5*0)+(4*8)+(3*0)+(2*4)+(1*1)=53
53 % 10 = 3
So 2080-41-3 is a valid CAS Registry Number.
2080-41-3Relevant articles and documents
Use of carbon-sulfur cathodes in electro-organic chemistry - Part 2 - Reactions with activated alkenes; evidence for a vicarious substitution specific of this type of electrode.
Guillanton, G. Le,Do, Q. T.,Simonet, J.
, p. 427 - 439 (2007/10/02)
The sulfur-carbon electrode, used as a cathode, appears to be an excellent source of nucleophiles which are good sulfuration reagents towards alkenes not substituted by leaving groups.However, the electrochemical reactions are often complex.It should be w
