5912-18-5 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
1H-Pyrrolo[2,3-b]pyridine, 4,6-dichlorois used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its potent biological activities make it a valuable component in the development of new drugs and pesticides.
Used in Cancer Research and Treatment:
1H-Pyrrolo[2,3-b]pyridine, 4,6-dichlorohas been studied for its potential anti-cancer properties. It is used as a research compound to explore its effects on cancer cells and to develop new therapeutic agents for cancer treatment.
Used in Inflammation and Pain Management:
Due to its anti-inflammatory properties, 1H-Pyrrolo[2,3-b]pyridine, 4,6-dichlorois used in the research and development of new drugs for inflammation and pain management.
Used in Organic Synthesis:
1H-Pyrrolo[2,3-b]pyridine, 4,6-dichloroserves as a precursor in the production of other organic compounds. Its unique structure and functional groups make it a versatile building block for the synthesis of various organic molecules.
Used in Materials Science:
In the field of materials science, 1H-Pyrrolo[2,3-b]pyridine, 4,6-dichlorohas applications in the development of organic semiconductors and optoelectronic devices. Its electronic properties and structural features contribute to the advancement of these technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 5912-18-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,1 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5912-18:
(6*5)+(5*9)+(4*1)+(3*2)+(2*1)+(1*8)=95
95 % 10 = 5
So 5912-18-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H4Cl2N2/c8-5-3-6(9)11-7-4(5)1-2-10-7/h1-3H,(H,10,11)
5912-18-5Relevant academic research and scientific papers
Synthesis of functionalized 7-azaindoles via directed ortho-metalations
L'Heureux, Alexandre,Thibault, Carl,Ruel, Réjean
, p. 2317 - 2319 (2007/10/03)
Functionalization at C-5 of 4-fluoro- and 4-chloro-1-triisopropylsilyl-7- azaindole, 1 and 2, respectively, leads to a variety of new substituted 7-azaindole derivatives. We also describe two approaches to introduce functionality at C-6.
