102210-80-0 Usage
Chemical class
Indole derivatives
Explanation
The compound has an indole ring as its core structure, with additional substituents.
Explanation
The indole ring is the central structure of the compound, with a hydrogen atom at the 1-position.
Explanation
The indole ring is substituted with two different groups, one at the 3-position and the other at the 1-position.
a. 3-(3-methyl-1-oxo-2-butenyl) group
Explanation
This group consists of a 2-butenyl chain with a 3-methyl-1-oxo (3-methyl-1-keto) functional group at the 3-position.
b. Phenylsulfonyl group
Explanation
This group is a phenyl ring attached to a sulfonyl (-SO2) functional group.
Explanation
The compound has potential biological activities, making it a candidate for further research and development in pharmaceuticals and drug discovery.
Explanation
The compound is frequently used in organic synthesis and pharmaceutical research due to its unique structure and potential applications.
Explanation
The compound's potential biological activities and unique structure make it a valuable resource in the development of new drugs and pharmaceutical compounds.
Indole ring
1H-Indole
Substituent groups
3-(3-methyl-1-oxo-2-butenyl) and phenylsulfonyl
Biological activities
Potential applications
Organic synthesis and pharmaceutical research
Common usage
Drug development
Applications in new drugs and pharmaceutical compounds
Check Digit Verification of cas no
The CAS Registry Mumber 102210-80-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,2,1 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 102210-80:
(8*1)+(7*0)+(6*2)+(5*2)+(4*1)+(3*0)+(2*8)+(1*0)=50
50 % 10 = 0
So 102210-80-0 is a valid CAS Registry Number.
102210-80-0Relevant academic research and scientific papers
Yuehchukene Analogues
Wenkert, Ernest,Moeller, Peter D. R.,Piettre, Serge R.,McPhail, Andrew T.
, p. 3170 - 3178 (2007/10/02)
Yuehchukene and the bisnoryuehchukenes have been synthesized by the dimerization of β-(dehydroprenyl)indole and its demethyl derivative, respectively.Several routes of preparation of the monomers were developed.These β-indolyl dienes were used in Diels-Al
Synthesis of Prenylated Indoles
Wenkert, Ernest,Angell, E. Charles,Ferreira, Vitor F.,Michelotti, Enrique L.,Piettre, Serge R.,et al.
, p. 2343 - 2351 (2007/10/02)
Interaction of magnesium indolates and allyl oxides in the presence of bis(triphenylphosphine)nickel dichloride results in indole β-allylation, except in cases involving highly substituted indoles and allyl alcohols.This method permits the β-prenylation of indole and α-prenylation of ketones (by way of their magnesium enaminates).Base-induced interaction of ethynyldimethylcarbinyl chloride and indole under a variety of conditions yields β-(β,β-dimethylvinyl)quinoline as well as variously dehydroprenylated indoles. α-Lithiation of N-(benzenesulfonyl)indole followed by treatmentwith prenyl bromide or β,β-dimethylacrylyl chloride produces α-prenyl- or α-oxoprenylidole derivatives, the sodium amalgam reduction of the former of which yields α-prenylidole.Interaction of β-cuprated N-(benzenesulfonyl)indole with the same halides followed by reduction affords β-prenylindole and β-oxoprenylindole, the latter also being the product of the reaction of magnesium indolate and the acid chloride.Lithium aluminum hydride reduction of 1-(benzenesulfonyl)-3-oxoprenylindole affords an alcohol, whose base hydrolysis produces β-dehydroprenylindole, a compound whose dimerization has led previously to naturally occuring yuehchukene.
