134031-25-7 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
(2,4-Dichloropyridin-3-yl)(phenyl)methanone is utilized as a building block for the synthesis of pharmaceuticals and agrochemicals. Its unique structure and reactivity contribute to the development of new compounds with potential therapeutic and pesticidal properties.
Used in Organic Synthesis:
(2,4-Dichloropyridin-3-yl)(phenyl)methanone serves as a precursor in organic synthesis, where it can be further modified or combined with other molecules to create a wide range of chemical products. Its versatility in chemical reactions makes it an essential component in the synthesis of various organic compounds.
Used in Chemical Compound Production:
(2,4-Dichloropyridin-3-yl)(phenyl)methanone is employed in the production of other chemical compounds, expanding its applications across different industries. Its role in the synthesis of new materials contributes to the advancement of various chemical processes.
Used in Material Development:
The chemical properties and reactivity of (2,4-Dichloropyridin-3-yl)(phenyl)methanone make it useful in the development of new materials. Its potential applications in material science can lead to the creation of innovative products with improved properties and performance.
However, it is crucial to handle (2,4-Dichloropyridin-3-yl)(phenyl)methanone with caution, as it may pose hazards to human health and the environment. Proper safety measures and disposal methods should be followed to minimize any potential risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 134031-25-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,0,3 and 1 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 134031-25:
(8*1)+(7*3)+(6*4)+(5*0)+(4*3)+(3*1)+(2*2)+(1*5)=77
77 % 10 = 7
So 134031-25-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H7Cl2NO/c13-9-6-7-15-12(14)10(9)11(16)8-4-2-1-3-5-8/h1-7H
134031-25-7Relevant articles and documents
Deprotonative metalation of chloro- and bromopyridines using amido-based bimetallic species and regioselectivity-computed CH acidity relationships
Snegaroff, Katia,Nguyen, Tan Tai,Marquise, Nada,Halauko, Yury S.,Harford, Philip J.,Roisnel, Thierry,Matulis, Vadim E.,Ivashkevich, Oleg A.,Chevallier, Floris,Wheatley, Andrew E. H.,Gros, Philippe C.,Mongin, Florence
experimental part, p. 13284 - 13297 (2012/02/03)
A series of chloro- and bromopyridines have been deprotometalated by using a range of 2,2,6,6-tetramethylpiperidino-based mixed lithium-metal combinations. Whereas lithium-zinc and lithium-cadmium bases afforded different mono- and diiodides after subsequent interception with iodine, complete regioselectivities were observed with the corresponding lithium-copper combination, as demonstrated by subsequent trapping with benzoyl chlorides. The obtained selectivities have been discussed in light of the CH acidities of the substrates, determined both in the gas phase and as a solution in THF by using the DFT B3LYP method.
