28995-86-0 Usage
Uses
Used in Organic Synthesis:
(Z)-2-iodo-2-phenylethenyl 1-methylethyl sulfone is utilized as a reagent in organic synthesis, where its specific properties and the presence of a phenyl ring, iodine atom, and double bond enable it to participate in a range of chemical reactions. (Z)-2-iodo-2-phenylethenyl 1-methylethyl sulfone's versatility in organic synthesis makes it a valuable tool for creating new molecules and compounds with potential applications in various industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (Z)-2-iodo-2-phenylethenyl 1-methylethyl sulfone can be used as a building block for the development of new drugs. Its unique structure and reactivity may allow for the creation of novel therapeutic agents with specific targeting capabilities or improved pharmacological properties.
Used in Chemical Research:
(Z)-2-iodo-2-phenylethenyl 1-methylethyl sulfone also has potential applications in chemical research, where it can be employed to study reaction mechanisms, explore new synthetic pathways, and investigate the effects of structural modifications on compound properties. This research can lead to a better understanding of chemical processes and the development of new materials and compounds with specific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 28995-86-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,9,9 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 28995-86:
(7*2)+(6*8)+(5*9)+(4*9)+(3*5)+(2*8)+(1*6)=180
180 % 10 = 0
So 28995-86-0 is a valid CAS Registry Number.
28995-86-0Relevant academic research and scientific papers
Synthesis of (E)-iodo vinylsulfones via oxidative addition of thiol into alkyne under metal free condition
Samanta, Surya Kanta,Sarkar, Rumpa,Bera, Mrinal K.
supporting information, (2021/07/12)
An efficient, transition-metal free and molecular iodine promoted protocol for the construction of (E)-β-iodovinyl sulfone derivatives via oxidative C–S coupling of thiol and alkyne has been demonstrated. Both aryl and alkyl terminal acetylenes were found to be an excellent substrate for the present reaction which provides a wide range of β-iodovinyl sulfone derivatives with very good yield and excellent regio and stereo-selectivities. Diaryldisulfide is also found to be an equally efficient sulfonyl group surrogate under identical reaction conditions.
