245064-82-8 Usage
Molecular Structure
The compound has a heterocyclic structure consisting of a pyrrolo[2,3-b]pyridine core and an ethyl ester group.
Functional Groups
The compound contains a carboxylic acid group, an ethyl ester group, and a phenylsulfonyl group.
Physical Properties
The physical properties of the compound are not provided in the material.
Chemical Reactivity
The presence of the phenylsulfonyl group makes the compound a valuable reagent in synthetic chemistry, particularly for the preparation of various pharmaceutical compounds and agrochemicals.
Potential Applications
The compound has potential applications as an intermediate in the synthesis of various bioactive compounds due to its unique structure and reactivity.
Versatility
1H-Pyrrolo[2,3-b]pyridine-3-carboxylic acid, 1-(phenylsulfonyl)-, ethyl ester is a versatile compound that has a wide range of uses in the chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 245064-82-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,5,0,6 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 245064-82:
(8*2)+(7*4)+(6*5)+(5*0)+(4*6)+(3*4)+(2*8)+(1*2)=128
128 % 10 = 8
So 245064-82-8 is a valid CAS Registry Number.
InChI:InChI=1/C16H14N2O4S/c1-2-22-16(19)14-11-18(15-13(14)9-6-10-17-15)23(20,21)12-7-4-3-5-8-12/h3-11H,2H2,1H3
245064-82-8Relevant articles and documents
Synthesis of benzo[5',6']cyclohepta[4,5]pyrrolo[2,3-b]pyridin-12-one
Mouaddib, Abderrahim,Joseph, Benoit,Hasnaoui, Aissa,Merour, Jean-Yves
, p. 5853 - 5854 (2007/10/03)
The synthesis of a 7-azaindole derivative 8 with potential antitumoral activity is described starting from pyrrolo[2,3-b]pyridine; regioselective lithiation/methylation of alkyl 7-azaindole-3-carboxylates 4 afforded the 2- methyl derivatives 5. Demethylat
