56970-92-4 Usage
Uses
Used in Chemical Research:
PYRIDIN-2-YL(PYRIDIN-4-YL)METHANONE is utilized as a key intermediate in chemical research for the synthesis of complex organic molecules. Its versatile structure allows for the development of new compounds with various applications.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, PYRIDIN-2-YL(PYRIDIN-4-YL)METHANONE serves as a crucial building block for the creation of new drugs. Its heterocyclic nature contributes to the design and synthesis of innovative medicinal compounds.
Used in Agrochemical Development:
PYRIDIN-2-YL(PYRIDIN-4-YL)METHANONE is also employed in the development of agrochemicals, where its structure can be leveraged to create new pesticides or other agricultural products.
Used in Medicinal Chemistry for Antimicrobial Applications:
PYRIDIN-2-YL(PYRIDIN-4-YL)METHANONE has been studied for its antimicrobial properties, making it a valuable compound in the search for new antibiotics and antifungal agents.
Used in Medicinal Chemistry for Antifungal Applications:
Similarly, its antifungal potential positions PYRIDIN-2-YL(PYRIDIN-4-YL)METHANONE as a candidate for the development of new treatments for fungal infections.
Check Digit Verification of cas no
The CAS Registry Mumber 56970-92-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,9,7 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 56970-92:
(7*5)+(6*6)+(5*9)+(4*7)+(3*0)+(2*9)+(1*2)=164
164 % 10 = 4
So 56970-92-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H8N2O/c14-11(9-4-7-12-8-5-9)10-3-1-2-6-13-10/h1-8H
56970-92-4Relevant academic research and scientific papers
Chen, Xu-Dong,Mak, Thomas C. W.
, p. 3529 - 3531 (2005)
An ordered sequence of the coordinating ability of a series of polyatomic monoanions has been established on the basis of structural parameters derived from their interaction with a disilver(i) metallacyclophane skeleton in isostructural complexes. The Royal Society of Chemistry 2005.
Preferential reactivity of pyridylmagnesiumchloride with n,n-dialkyl arylamides over carbonitriles: Synthesis of 2-(Aroyl) pyridines
Rao, G. Venkateswara,Swamy, B. Narayana,Kumar, P. Hareesh,Reddy, G. Chandrasekara
experimental part, p. 1835 - 1846 (2009/11/30)
Reaction of 2-pyridylmagnesium chlorides with N,N-dialkyl arylamides afford exclusively 2-(aroyl) pyridines in high yields and purity without the formation of any tertiary alcohol. This method employs easily available raw materials and avoids the use of h
