21961-10-4 Usage
Uses
Used in Organic Synthesis:
(Vinylsulfonyl)cyclohexane is used as a building block in organic synthesis for introducing the vinylsulfonyl group into different molecules. The presence of this group facilitates cross-coupling reactions and other organic transformations, enhancing the compound's reactivity and synthetic utility.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (vinylsulfonyl)cyclohexane is utilized as a precursor for the synthesis of pharmaceutical intermediates. Its unique structure and functional group make it a suitable candidate for the development of new drugs and therapeutic agents, contributing to the advancement of medicinal chemistry.
Used in Chemical Research:
(Vinylsulfonyl)cyclohexane also finds application in chemical research, where it can be employed to study the properties and reactivity of the vinylsulfonyl group. This understanding can lead to the discovery of new reaction pathways and the development of innovative synthetic strategies in organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 21961-10-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,9,6 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 21961-10:
(7*2)+(6*1)+(5*9)+(4*6)+(3*1)+(2*1)+(1*0)=94
94 % 10 = 4
So 21961-10-4 is a valid CAS Registry Number.
21961-10-4Relevant academic research and scientific papers
Diastereoselective Monofluorocyclopropanation Using Fluoromethylsulfonium Salts
Melngaile, Renate,Sperga, Arturs,Baldridge, Kim K.,Veliks, Janis
, p. 7174 - 7178 (2019/09/12)
Diarylfluoromethylsulfonium salts, alternatives to freons or advanced fluorinated building blocks, are bench stable and easy-to-use sources of direct fluoromethylene (:CHF) transfer to alkenes. These salts enabled development of a trans-selective monofluorinated Johnson-Corey-Chaykovsky reaction with vinyl sulfones or vinyl sulfonamides to access synthetically challenging monofluorocyclopropane scaffolds. The described method offers rapid access to monofluorinated cyclopropane building blocks with further functionalization opportunities to deliver more complex synthetic targets diastereoselectively.
Fused benzo compounds containing a nitrogen heterocycle for the treatment of central nervous system disorders
-
, (2008/06/13)
Fused benzo compounds of formula I are provided, wherein A is a 2 to 6 membered hydrocarbon spacer group, B is a polar divalent group selected from a group (a); U is C, N or CH; X is a divalent 3-4 membered chain optionally comprising one or more heteroat
