1353056-43-5 Usage
Uses
Used in Organic Synthesis:
2,3-Dibromo-4-iodopyridine serves as a building block in organic synthesis, facilitating the creation of more complex molecules. Its presence in the synthesis process is crucial for developing a range of chemical products.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 2,3-Dibromo-4-iodopyridine is used as a key intermediate in the synthesis of drugs. Its unique properties make it a valuable component in the development of new medicinal compounds.
Used in Agrochemical Production:
2,3-Dibromo-4-iodopyridine also finds application in the agrochemical sector, where it is used in the synthesis of pesticides and other agricultural chemicals, contributing to the development of effective crop protection agents.
Used in Materials Science:
2,3-Dibromo-4-iodopyridine is utilized in materials science for the synthesis of new materials with specific properties, such as those with potential applications in electronics or advanced materials research.
Used as a Reagent in Chemical Research:
In the realm of chemical research, 2,3-Dibromo-4-iodopyridine is an important reagent. It is used as a precursor in various chemical reactions, enabling the synthesis of new chemical entities and contributing to the advancement of synthetic chemistry.
Used in Metal-Catalyzed Transformations:
2,3-Dibromo-4-iodopyridine also plays a significant role in metal-catalyzed transformations, where it can act as a substrate to produce a variety of chemical products, thereby expanding the scope of synthetic methodologies in chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 1353056-43-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,3,0,5 and 6 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1353056-43:
(9*1)+(8*3)+(7*5)+(6*3)+(5*0)+(4*5)+(3*6)+(2*4)+(1*3)=135
135 % 10 = 5
So 1353056-43-5 is a valid CAS Registry Number.
1353056-43-5Relevant academic research and scientific papers
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.
