65147-89-9 Usage
General Description
6-BROMO-2-PHENYL-1H-IMIDAZO[4,5-B]PYRIDINE is a chemical compound with the molecular formula C13H8BrN3. It is a heterocyclic organic compound with a fused imidazopyridine ring system. This chemical is commonly used in the synthesis of pharmaceuticals and is known for its potential biological activity. Its structure and properties make it a valuable building block in the development of drug candidates for various therapeutic targets. Additionally, it is often used as a reagent in organic synthesis and medicinal chemistry research due to its unique molecular structure and functional groups.
Check Digit Verification of cas no
The CAS Registry Mumber 65147-89-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,1,4 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 65147-89:
(7*6)+(6*5)+(5*1)+(4*4)+(3*7)+(2*8)+(1*9)=139
139 % 10 = 9
So 65147-89-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H8BrN3/c13-9-6-10-12(14-7-9)16-11(15-10)8-4-2-1-3-5-8/h1-7H,(H,14,15,16)
65147-89-9Relevant articles and documents
Unambiguous structural assignment of monoanils obtained from 2,3-pyridinediamines
Dubey,Kumar, R. Vinod,Kulkarni, Subhash M.,Sunder, G. Hema,Smith, Graham,Kennard, Collin H. L.
, p. 952 - 956 (2007/10/03)
The reaction of 2,3-pyridinediamine la and its 5-bromo analogue lb independently with aromatic aldehydes results in the formation of 2-amino-and 5-bromo-2-amino-3-arylideneaminopyridines (2a and 2b) respectively. The structure of 2 has been confirmed by single crystal X-ray analysis, thereby ruling out the alternate structure for these compounds.
Structure and reactions of monoanils obtained from 2,3-pyridinediamines
Dubey,Kulkarni,Vinod Kumar
, p. 361 - 367 (2007/10/03)
The reaction of 2,3-pyridinediamines 1 with aromatic aldehydes results in the formation of 2-amino-3-arylideneaminopyridines 2 respectively. Dehydrogenative cyclisation of 2 with different reagents give 2-aryl-1H-imidazo[4,5-b]pyridines 4. Reactions of 2 with different reagents have been described.
