281192-96-9 Usage
Heterocyclic compound
The compound has a pyrrolopyridine core, which is a structure containing both pyrrole and pyridine rings.
Phenylmethyl substituent
The compound has a phenylmethyl group attached to the pyrrolopyridine core, which is a benzene ring with a methyl group attached to it.
Medicinal chemistry building block
The compound is used as a building block in the synthesis of various pharmaceutical compounds, particularly in the development of potential drug candidates.
Potential pharmacological activities
The compound has been studied for its potential anti-inflammatory, anti-cancer, and anti-viral properties.
Unique structure and reactivity
The compound's structure and reactivity make it a valuable intermediate for the creation of diverse chemical entities with potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 281192-96-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,1,1,9 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 281192-96:
(8*2)+(7*8)+(6*1)+(5*1)+(4*9)+(3*2)+(2*9)+(1*6)=149
149 % 10 = 9
So 281192-96-9 is a valid CAS Registry Number.
281192-96-9Relevant articles and documents
AlCl3/PCC-SiO2-promoted oxidation of azaindoles and indoles
Sriram, Rekulapally,Sesha Sai Pavan Kumar, Chebolu Naga,Raghunandan, Nerella,Ramesh, Vadla,Sarangapani, Manda,Rao, Vaidya Jayathirtha
experimental part, p. 3419 - 3428 (2012/09/22)
A simple and efficient method is described for the oxidation of 7-azaindoles and indoles to 7-azaisatins and isatins using pyridinium chlorochromate-silica gel (PCC-SiO2) with the aid of Lewis acid catalyst aluminium chloride (AlCl3) in dichloroethane. Simplicity of the reaction conditions, easy workup procedure, and good yields are the key features of this protocol.
A facile synthesis of 1-alkyl-7-azaisatins
Tatsugi, Jiro,Zhiwei, Tong,Amano, Tomohiro,Izawa, Yasuji
, p. 1145 - 1150 (2007/10/03)
1-Alkyl-7-azaisatins are synthesized from the reaction of 1-alkyl-7- azaindoles with bromine in dichloromethane and subsequent oxidation with N- bromosuccinimide - dimethyl sulfoxide reagent. 1-Alkyl-7-azaindoles are readily available in high yields from
