55304-86-4 Usage
General Description
2,6-dibromo-5-chloronicotinic acid is a chemical compound with the molecular formula C6H3Br2ClNO2. It belongs to the class of organic compounds known as pyridine carboxylic acids and derivatives. 2,6-dibroMo-5-chloronicotinic acid is a halogenated derivative of nicotinic acid, which is a precursor for the coenzyme β-nicotinamide adenine dinucleotide (NAD). 2,6-dibromo-5-chloronicotinic acid is mainly used in the pharmaceutical industry for the synthesis of various drugs and also has potential applications in the field of agrochemicals as a pesticide intermediate. It possesses both bromine and chlorine atoms, making it useful in organic synthesis for the formation of complex molecules. Additionally, it may have potential uses in other fields such as materials science and chemical research.
Check Digit Verification of cas no
The CAS Registry Mumber 55304-86-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,3,0 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 55304-86:
(7*5)+(6*5)+(5*3)+(4*0)+(3*4)+(2*8)+(1*6)=114
114 % 10 = 4
So 55304-86-4 is a valid CAS Registry Number.
55304-86-4Relevant articles and documents
Continuous process for the production of polybromopyridine compounds
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, (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.