56181-38-5 Usage
Uses
Used in Pharmaceutical Industry:
5-Bromo-N-methylpyrimidin-4-amine is used as a chemical intermediate for the synthesis of various pharmaceuticals. It plays a crucial role in the development of new drugs, contributing to the advancement of medicinal chemistry and therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 5-Bromo-N-methylpyrimidin-4-amine is utilized as an intermediate in the production of agrochemicals. Its involvement in the synthesis of these compounds aids in the development of innovative solutions for agricultural challenges, such as pest control and crop protection.
Used in Research and Development:
5-Bromo-N-methylpyrimidin-4-amine is employed in research and development for exploring its potential applications in both the pharmaceutical and agricultural industries. Its versatility as a chemical building block allows scientists to investigate its properties and reactivity, leading to the discovery of novel compounds and applications.
It is essential to handle 5-Bromo-N-methylpyrimidin-4-amine with care and follow safety guidelines to mitigate the potential hazards and risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 56181-38-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,1,8 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 56181-38:
(7*5)+(6*6)+(5*1)+(4*8)+(3*1)+(2*3)+(1*8)=125
125 % 10 = 5
So 56181-38-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H6BrN3/c1-7-5-4(6)2-8-3-9-5/h2-3H,1H3,(H,7,8,9)
56181-38-5Relevant academic research and scientific papers
Bromination of Some Pyridine and Diazine N-Oxides
Paudler, William W.,Jovanovic, Misa V.
, p. 1064 - 1069 (2007/10/02)
Selected monosubstituted pyridines, pyrazines, pyrimidines, and their N-oxides, having an electron-donating substituent, were successfully brominated under very mild conditions.The N-oxide function itself is not sufficient to cause these ?-deficient systems to undergo electrophilic aromatic halogenation.Only strongly electron-donating substituents (amino groups) activate the heterocyclic nucleus toward bromination.These substituents direct the electrophilic substitution ortho/para to them with or without the N-oxide group present.Pyridine and diazines with moderately activating substituents such as alkoxy groups are brominated only when their ortho/para activation is augmented by the activation of the N-oxide funtion.Failure to brominate 5-methoxypyrimidine 1-oxide may well reflect the greater ? deficiency of the pyrimidine ring.
