102839-50-9 Usage
Bicyclic heterocyclic compound
Pyridine ring fused to a pyrrole ring The structure of 1H-Pyrrolo[3,2-c]pyridine,1,4-dimethyl-(9CI) is formed by the fusion of two different heterocyclic rings, a pyridine ring, and a pyrrole ring.
Derivative of pyrrolopyridine
Modified version of the parent compound 1H-Pyrrolo[3,2-c]pyridine,1,4-dimethyl-(9CI) is derived from the parent compound pyrrolopyridine, with modifications in its structure.
Two methyl groups attached
At the 1 and 4 positions of the pyrrole ring This compound has two methyl groups (CH3) attached to specific positions on the pyrrole ring, which are the 1st and 4th positions, influencing its chemical properties and reactivity.
Potential pharmaceutical applications
Development of new drugs and medicinal compounds Due to its unique structure and properties, 1H-Pyrrolo[3,2-c]pyridine,1,4-dimethyl-(9CI) has potential uses in the pharmaceutical industry, particularly in the creation of new drugs and medicinal compounds.
Target for research and development
Organic and medicinal chemistry The distinct structure and properties of 1H-Pyrrolo[3,2-c]pyridine,1,4-dimethyl-(9CI) make it an interesting subject for research and development in the fields of organic chemistry and medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 102839-50-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,8,3 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 102839-50:
(8*1)+(7*0)+(6*2)+(5*8)+(4*3)+(3*9)+(2*5)+(1*0)=109
109 % 10 = 9
So 102839-50-9 is a valid CAS Registry Number.
102839-50-9Relevant articles and documents
4-Substituted-1-methyl-1H-pyrrolopyridines
Casy, Alan F.,Needle, Richard J.,Upton, Christopher
, p. 343 - 360 (2007/10/02)
The synthesis of a series of 4-substituted 1-methyl-1H-pyrrolopyridines is described based on transformations of 4-methyl and 4-chloro analogues.Reactivities of the latter compounds proved less than those of corresponding α-substituted pyridines, but pressure methods allowed isolation of the 4-amino and other amine derivatives in good yield.Under Mannich conditions both 4-methyl and 4-chloro derivatives were converted to bis methanes.
