143774-55-4 Usage
Indole derivative
Heterocyclic organic compound
A compound that is derived from the indole structure, which is a heterocyclic (having a ring with one or more non-carbon atoms) organic compound.
Bromomethyl group
Attached to the indole ring
A functional group consisting of a bromine atom bonded to a methyl group (one carbon atom with three hydrogen atoms), which is attached to the indole ring of the compound.
Phenylsulfonyl group
Attached to the indole ring
A functional group composed of a phenyl ring (a six-membered carbon ring with delocalized electrons) bonded to a sulfonyl group (a sulfur atom double-bonded to two oxygen atoms), which is attached to the indole ring of the compound.
Acetyl group
Position 3 of the indole ring
A functional group consisting of a carbonyl group (a carbon atom double-bonded to an oxygen atom) bonded to a methyl group (one carbon atom with three hydrogen atoms), which is located at the 3rd position of the indole ring.
Potential applications
Organic synthesis and medicinal chemistry
The compound may have possible uses in the fields of organic synthesis (the creation of new organic compounds) and medicinal chemistry (the study of compounds for potential pharmaceutical applications).
Safety precautions
Handle and use with care
As with all potentially hazardous chemicals, it is important to handle and use 1H-Indole, 3-acetyl-2-(bromomethyl)-1-(phenylsulfonyl)with appropriate safety measures to minimize risks to health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 143774-55-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,7,7 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 143774-55:
(8*1)+(7*4)+(6*3)+(5*7)+(4*7)+(3*4)+(2*5)+(1*5)=144
144 % 10 = 4
So 143774-55-4 is a valid CAS Registry Number.
143774-55-4Relevant articles and documents
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
Synthesis of di-, tri-, and tetra-substituted carbazole analogs involving annulation methodology
Ramesh, Neelamegam,Rajeshwaran, Ganesan Gobi,Mohanakrishnan, Arasambattu K.
experimental part, p. 3592 - 3602 (2009/09/06)
Synthesis of substituted carbazole analogs was achieved via Michael addition followed by intramolecular cyclization and subsequent aromatization.
An efficient preparation of 1-phenylsulfonylindolyl methyl sulfoxides using KF/m-CPBA
Mohanakrishnan, Arasambattu K.,Ramesh, Neelamegam
, p. 4231 - 4233 (2007/10/03)
A variety of 1-phenylsulfonylindolylmethyl sulfides are selectively oxidized to the corresponding sulfoxides using a hitherto unexplored KF/m-CPBA system. A major advantage is the absence of over-oxidation.
