189882-32-4 Usage
General Description
6-IODO-1H-PYRROLO[2,3-B]PYRIDINE is a chemical compound with the molecular formula C8H6IN. It is classified as a substituted pyrrolopyridine, containing a pyrrolo[2,3-b]pyridine core with an iodine atom attached at the 6-position. 6-IODO-1H-PYRROLO[2,3-B]PYRIDINE is primarily used in pharmaceutical research and development, as it exhibits potential for drug discovery and design. It may also be employed as a building block in the synthesis of other complex organic molecules. Furthermore, 6-IODO-1H-PYRROLO[2,3-B]PYRIDINE has shown promise in the field of medicinal chemistry, displaying biological activity that is of interest for the development of new therapeutic agents. Its unique structure and properties make it a valuable and versatile chemical for various scientific and commercial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 189882-32-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,8,8 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 189882-32:
(8*1)+(7*8)+(6*9)+(5*8)+(4*8)+(3*2)+(2*3)+(1*2)=204
204 % 10 = 4
So 189882-32-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H5IN2/c8-6-2-1-5-3-4-9-7(5)10-6/h1-4H,(H,9,10)
189882-32-4Relevant articles and documents
Synthesis and Biological Activity of 1H-Pyrrolo[2,3-b]pyridine Derivatives: Correlation between Inhibitory Activity against the Fungus Causing Rice Blast and Ionization Potential
Minakata, Satoshi,Hamada, Takayuki,Komatsu, Mitsuo,Tsuboi, Hiroyuki,Kikuta, Hiroshige,Ohshiro, Yoshiki
, p. 2345 - 2348 (1997)
Synthesis and biological activity of a variety of 3- and 6-substituted 1H-pyrrolo[2,3-6]pyridine (7-azaindole) derivatives are described. Many of the synthesized 7-azaindoles exhibited considerable fungicidal activity toward Pyricularia oryzae, a fungus which causes rice blast, in vivo. When quantum parameters of the tested 7-azaindoles were evaluated by semiempirical molecular orbital calculations, a relationship was observed between the activity and the calculated ionization potentials of the 7-azaindole derivatives.
