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56181-38-5

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56181-38-5 Usage

General Description

5-Bromo-N-methylpyrimidin-4-amine is a chemical compound with the molecular formula C5H6BrN3. It is a derivative of pyrimidine and belongs to the class of amines. This chemical is used as an intermediate for the synthesis of pharmaceuticals and agrochemicals. It is also used in research and development for various applications in the pharmaceutical and agricultural industries. The compound is known for its potential as a building block in the development of new drugs and agrochemical products. It is important to handle this chemical with care and in accordance with safety guidelines due to its 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)

56181-38-5Upstream product

56181-38-5Downstream Products

56181-38-5Relevant articles and documents

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.

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