50850-04-9 Usage
Uses
Used in Pharmaceutical and Biological Applications:
1-(4-chlorophenyl)-3,3-disulfanylprop-2-en-1-one is used as a compound with potential pharmaceutical and biological applications due to its antimicrobial, antioxidant, and anticancer properties. Its ability to combat various diseases and promote overall health makes it a valuable asset in the development of new drugs and therapies.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(4-chlorophenyl)-3,3-disulfanylprop-2-en-1-one is used as a key intermediate for the synthesis of various complex organic molecules. Its unique structure and functional groups make it a versatile building block for creating a wide range of compounds with diverse applications.
Used in Drug Development:
Due to its structural similarity to curcumin, 1-(4-chlorophenyl)-3,3-disulfanylprop-2-en-1-one is used as a potential natural product-based drug lead for the treatment of various diseases. Its promising properties and potential therapeutic applications make it an attractive candidate for further research and development in the pharmaceutical industry.
Used in Antimicrobial Applications:
1-(4-chlorophenyl)-3,3-disulfanylprop-2-en-1-one is used as an antimicrobial agent for its ability to inhibit the growth of harmful microorganisms. This property makes it a valuable tool in the development of new antimicrobial drugs and treatments, particularly in the face of increasing antibiotic resistance.
Used in Antioxidant Applications:
As an antioxidant, 1-(4-chlorophenyl)-3,3-disulfanylprop-2-en-1-one is used to neutralize harmful free radicals and protect cells from oxidative damage. Its antioxidant properties make it a potential candidate for use in the development of new therapies and supplements aimed at promoting overall health and longevity.
Used in Anticancer Applications:
1-(4-chlorophenyl)-3,3-disulfanylprop-2-en-1-one is used as a potential anticancer agent due to its ability to target and inhibit the growth of cancer cells. Its potential to be developed into a novel cancer treatment makes it an important compound for further research and development in the field of oncology.
Check Digit Verification of cas no
The CAS Registry Mumber 50850-04-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,8,5 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 50850-04:
(7*5)+(6*0)+(5*8)+(4*5)+(3*0)+(2*0)+(1*4)=99
99 % 10 = 9
So 50850-04-9 is a valid CAS Registry Number.
50850-04-9Relevant academic research and scientific papers
Synthesis of densely substituted 1,3-butadienes through acid-catalyzed alkenylations of α-oxoketene dithioacetals with aldehydes
Liu, Changhui,Gu, Yanlong
supporting information, p. 9619 - 9627 (2015/01/09)
Aldehydes were proved to be viable reagents for implementing alkenylation of α-oxoketene dithioacetals. AlCl3 was found to be the best catalyst. The established reaction opened an avenue to access densely substituted 1,3-butadiene derivatives. The obtained product bears multiple reactive sites that can be converted into various valuable molecules. (Chemical Equation Presented).
Discovery of a new class of protein farnesyltransferase inhibitors in the arylthiophene series
Lethu, Sébastien,Ginisty, Maryon,Bosc, Damien,Dubois, Jo?lle
supporting information; experimental part, p. 6205 - 6208 (2010/03/24)
Screening of the ICSN chemical library led to the discovery of 3-(4-chlorophenyl)-4-cyano-5-thioalkylthiophene 2-carboxylic acids as potent farnesyltransferase inhibitors. Enzymatic kinetic studies showed that this original FTI series belongs to the CaaX
