41789-38-2 Usage
Uses
Used in Organic Synthesis:
2,6-DIBROMO-3-(BROMOMETHYL)PYRIDINE is used as a building block in organic synthesis for the creation of a wide range of chemical compounds. Its unique structure allows for various chemical reactions, making it a key component in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2,6-DIBROMO-3-(BROMOMETHYL)PYRIDINE is utilized as an intermediate for the development of biologically active molecules. Its presence in the molecular structure can contribute to the pharmacological properties of potential drugs, thus playing a crucial role in drug discovery and design.
Safety Considerations:
It is important to handle 2,6-DIBROMO-3-(BROMOMETHYL)PYRIDINE with caution due to its hazardous nature. Exposure to 2,6-DIBROMO-3-(BROMOMETHYL)PYRIDINE may result in irritation to the skin, eyes, and respiratory system. Proper safety measures, including the use of personal protective equipment and adherence to safety protocols, are essential when working with this chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 41789-38-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,7,8 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 41789-38:
(7*4)+(6*1)+(5*7)+(4*8)+(3*9)+(2*3)+(1*8)=142
142 % 10 = 2
So 41789-38-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H4Br3N/c7-3-4-1-2-5(8)10-6(4)9/h1-2H,3H2
41789-38-2Relevant academic research and scientific papers
Continuous process for the production of polybromopyridine compounds
-
, (2008/06/13)
A continuous process for producing a polybromopyridine compound comprises admixing a polychloropyridine compound with an anhydrous water soluble solvent in a first reaction zone to form a solution of the polychloropyridine compound. Hydrogen bromide gas is introduced into the solution while maintaining the temperature in the range of from about 70° to about 140° C. to produce a solution of the polybromopyridine compound. The solution is cooled to a temperature in the range of from about 5° to about 35° C. to precipitate the polybromopyridine compound from the anhydrous solvent. The polybromopyridine compound is separated from the anhydrous solvent and the anhydrous solvent is returned to the first reaction zone. Polybromopyridine compounds of increased purity are produced in a process having reduced material, energy and operating costs. The process does not require the use of water or other co-solvents nor the distillation of the reaction product mixture.
