130103-64-9 Usage
Molecular Structure
1H-Indole, 7-(1-methylethyl)-1-(phenylsulfonyl)has a complex molecular structure that includes an indole ring, a 7-(1-methylethyl) substituent, and a phenylsulfonyl group.
Indole Ring
The compound contains an indole ring, which is a bicyclic structure consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing ring.
Substituents
The indole ring has a 7-(1-methylethyl) substituent, which is a methyl group (-CH3) attached to the carbon atom at the 7-position of the indole ring.
Phenylsulfonyl Group
The compound also features a phenylsulfonyl group (-SO2Ph), which is a sulfonyl group (-SO2) connected to a phenyl ring (a six-membered ring with alternating single and double bonds).
Organic Synthesis
1H-Indole, 7-(1-methylethyl)-1-(phenylsulfonyl)is often used in organic synthesis, making it a valuable compound for creating new chemical entities.
Pharmaceutical Research
Due to its potential biological activity, 1H-Indole, 7-(1-methylethyl)-1-(phenylsulfonyl)- is frequently utilized in pharmaceutical research for the development of new drugs or as a reagent in chemical reactions.
Medicinal and Biological Applications
The presence of the phenylsulfonyl group suggests that 1H-Indole, 7-(1-methylethyl)-1-(phenylsulfonyl)- may have significant potential for medicinal and biological applications.
Importance in Research
As a result of its potential applications and complex structure, 1H-Indole, 7-(1-methylethyl)-1-(phenylsulfonyl)is an important area of study for researchers in the pharmaceutical and chemical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 130103-64-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,1,0 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 130103-64:
(8*1)+(7*3)+(6*0)+(5*1)+(4*0)+(3*3)+(2*6)+(1*4)=59
59 % 10 = 9
So 130103-64-9 is a valid CAS Registry Number.
130103-64-9Relevant academic research and scientific papers
Diels-Alder reactions of 1,5-dihydropyrano[3,4-b]pyrrol-5(1H)-ones, pyrrole-2,3-quinodimethane analogues; a new synthesis of indoles
Mark Jackson,Moody, Christopher J.
, p. 7447 - 7466 (2007/10/02)
The pyrano[3,4-b]pyrrol-5-(1H)-ones 7 are stable cyclic analogues of pyrrole-2,3-quinodimethane, and undergo Diels-Alder reaction with a range of acetylenes (dimethyl acetylenedicarboxylate, ethyl propiolate, ethyl trimethylsilylpropynoate, benzyne and the acetylene equivalent, phenyl vinyl sulfoxide), to give, after loss of carbon dioxide, indoles. The Diels-Alder reaction can be extended to the intramolecular variant to give cycloalka-[e]- and [g]-indoles.
Diels-Alder Reactions of 2,3-Dimethylenepyrrole Analogues; a New Synthesis of Indoles
Jackson, P. Mark,Moody, Christopher J.
, p. 2156 - 2158 (2007/10/02)
The pyranopyrrol-5(1H)-ones (4) are stable cyclic analogues of 2,3-dimethylenepyrrole and undergo Diels-Alder reaction with a range of acetylenes, or acetylene equivalents, to give, after loss of carbon dioxide, indoles.
