113685-33-9 Usage
Molecular structure
1H-Indole, 3-acetyl-2-methyl-1-(phenylsulfonyl)is a complex organic compound that contains an indole ring with various substituent groups.
Indole ring
The compound contains an indole ring, which is a tricyclic aromatic system consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring.
Acetyl group
The compound has an acetyl group (-COCH3) attached to the 3 position of the indole ring, which is an important functional group in organic chemistry.
Methyl group
The compound has a methyl group (-CH3) attached to the 2 position of the indole ring, which is a common alkyl group.
Phenylsulfonyl group
The compound has a phenylsulfonyl group (-SO2C6H5) attached to the 1 position of the indole ring, which is a derivative of benzene with a sulfonyl group (-SO2H) attached to it.
Potential building block
The presence of the acetyl and phenylsulfonyl groups makes 1H-Indole, 3-acetyl-2-methyl-1-(phenylsulfonyl)a potential building block for the synthesis of various organic compounds.
Pharmaceutical applications
1H-Indole, 3-acetyl-2-methyl-1-(phenylsulfonyl)has potential applications in the pharmaceutical industry for the development of new drug molecules.
Research tool
The compound can be used as a research tool in organic chemistry and medicinal chemistry for the exploration of new chemical reactions and biological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 113685-33-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,6,8 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 113685-33:
(8*1)+(7*1)+(6*3)+(5*6)+(4*8)+(3*5)+(2*3)+(1*3)=119
119 % 10 = 9
So 113685-33-9 is a valid CAS Registry Number.
113685-33-9Relevant academic research and scientific papers
Synthesis and Biological Evaluation of Calothrixins B and their Deoxygenated Analogues
Muthu Ramalingam, Bose,Dhatchana Moorthy, Nachiappan,Chowdhury, Somenath Roy,Mageshwaran, Thiyagarajan,Vellaichamy, Elangovan,Saha, Sourav,Ganesan, Karthikeyan,Rajesh, B. Navin,Iqbal, Saleem,Majumder, Hemanta K.,Gunasekaran, Krishnasamy,Siva, Ramamoorthy,Mohanakrishnan, Arasambattu K.
, p. 1285 - 1315 (2018/02/17)
A series of calothrixin B (2) analogues bearing substituents at the 'E' ring and their corresponding deoxygenated quinocarbazoles lacking quinone unit were synthesized. The cytotoxicities of calothrixins 1, 2, and 15b-p and quinocarbazole analogues were i
Unusual acetylation of 2-methyl-1-phenylsulfonylindole
Merour, Jean-Yves,Malapel, Beatrice,Desarbre, Eric
, p. 3267 - 3276 (2007/10/03)
Acetylation of 2-methyl-1-phenylsulfonylindole with an excess of aluminium chloride and acetic anhydride afforded exclusively 6-acetyl-3-chloro-2-methylindole and 6-acetyl-3-chloro-2-methyl-1-phenylsulfonylindole.
Synthesis and cycloaddition of 2,4-dihydropyrroloindoles
Jeevanandam, Arumugasamy,Srinivasan, Panayencheri C.
, p. 2663 - 2666 (2007/10/02)
Friedel-Crafts acylation of 2-methyl-1-phenylsulfonylindole 6 gave the 3-acyl derivatives 7 which upon side chain bromination with N-bromosuccinimide (NBS) followed by treatment with primary amines afforded the title compounds 9.Diels-Alder reaction of 9 with dimethyl acetylenedicarboxylate (DMAD) gave the polysubstituted carbazoles 12.
