82447-90-3 Usage
Heterocyclic compound
The compound contains atoms of different elements (heteroatoms) in its ring structure, specifically nitrogen atoms in this case.
Pyrrolopyridine structure
The compound has a fused pyrrole and pyridine ring system, which is a common structural motif in many biologically active molecules.
Carbonitrile group
A cyano group (C≡N) is present in the molecule, which is a strong electron-withdrawing group and can influence the reactivity and properties of the compound.
Amino group
The presence of an amino group (-NH2) in the molecule provides a source of hydrogen bonding and can participate in various chemical reactions.
Pharmaceutical industry use
1H-Pyrrolo[3,2-c]pyridine-7-carbonitrile, 6-amino-2,3-dihydro- is commonly used as a building block for the synthesis of various bioactive molecules, particularly in the development of potential drug candidates.
Valuable intermediate
Due to its unique structure and functional groups, the compound is a valuable intermediate in the production of pharmaceuticals and other organic compounds.
Potential applications in medicinal chemistry and drug discovery
The interesting chemical properties of 1H-Pyrrolo[3,2-c]pyridine-7-carbonitrile, 6-amino-2,3-dihydro- make it a promising candidate for further research and development in the fields of medicinal chemistry and drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 82447-90-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,4,4 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 82447-90:
(7*8)+(6*2)+(5*4)+(4*4)+(3*7)+(2*9)+(1*0)=143
143 % 10 = 3
So 82447-90-3 is a valid CAS Registry Number.
82447-90-3Relevant academic research and scientific papers
Granik,Zhidkova,Dubinskii
, p. 395 - 400 (1982)
The synthesis of 2,3,5,6-tetrahydropyrrolo[3,2-c]pyrid-6-one was accomplished by rearrangement of 8H,1-cyano-8-dimethylaminomethylene-2,5,6,7-tetrahydropyrrolo[1, 2-c]pyrimidine. Pyrrolo[3,2-c]pyrimidine, 1,6-naphthyridine, and pyrimido[4,3-b]-azepine derivatives were synthesized on the basis of enamino dinitriles. The hydrolysis of 8H,1-cyano-8-dimethylaminomethylene-2,5,6,7-tetrahydropyrrolo[1,2-c]-pyrimidine in 50% CH3COOH leads to a pyrrolo[1,2-c]pyrido[4′,3′-d]pyrimidine derivative. A similar dipyrido[4,3-d-1′,2′-c]pyrimidine derivative was obtained from 1-cyano-9-dimethylaminomethylene-2,5,6,7,8,9-hexahydropyrido[1,2-c]pyrimidine under these conditions, and 3,4-dioxo-3,4,7,8,9,10-hexahydropyrido[1,2-c]pyrano[4′,3′-d]-pyrimidine was synthesized bytreatment with a 1 N solution of HCl.
