97653-12-8

Basic information

• Product Name: N-(4,6-dimethylpyrimidin-2-yl)-N-(2-oxo-2-phenylethyl)cyanamide
• Synonyms: N-(4,6-dimethylpyrimidin-2-yl)-N-(2-oxo-2-phenylethyl)cyanamide
• CAS NO: 97653-12-8
• Molecular Weight: 266.302
• Mol File: 97653-12-8.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: N-(4,6-dimethylpyrimidin-2-yl)-N-(2-oxo-2-phenylethyl)cyanamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4,6-dimethylpyrimidin-2-yl)-N-(2-oxo-2-phenylethyl)cyanamide(97653-12-8)
• EPA Substance Registry System: N-(4,6-dimethylpyrimidin-2-yl)-N-(2-oxo-2-phenylethyl)cyanamide(97653-12-8)

Safety Data

• Hazardous Substances Data: 97653-12-8(Hazardous Substances Data)

Upstream product

• 97653-11-7 5,7-dimethyl-3-phenacyl<1,2,4>triazolo<1,5-a>pyrimidinium bromide 
• 55474-90-3 (4,6-dimethylpyrimidin-2-yl)cyanamide 
• 70-11-1 α-bromoacetophenone 
• 7681-99-4 5,7-dimethyl-[1,2,4]triazolo[1,5-a]pyrimidine 
• 922-67-8 propynoic acid methyl ester 

Downstream Products

• 104499-07-2 2-[1-(4,6-Dimethyl-pyrimidin-2-yl)-4-phenyl-1H-imidazol-2-ylamino]-ethanol 
• 104499-06-1 2-(2-i-propyloxy-4-phenylimidazolyl)-4,6-dimethylpyrimidine 
• 104499-05-0 2-(2-methoxy-4-phenylimidazolyl)-4,6-dimethylpyrimidine 
• 97653-16-2 2-(2-diethylamino-4-phenylimidazolyl)-4,6-dimethylpyrimidine 
• 97653-15-1 2-(2-ethoxy-4-phenylimidazolyl)-4,6-dimethylpyrimidine 
• 97653-14-0 4,6-dimethyl-2-(2-oxo-5-phenyloxazol-3-yl)pyrimidine 
• 97653-13-9 2-(2-imino-5-phenyl-2,3-dihydro-oxazol-3-yl)-4,6-dimethylpyrimidine 

Relevant articles and documents

Detailed Studies of the Alkylation Sides of Pyridin-2-yl and 4,6-Dimethylpyrimidin-2-yl-cyanamides

Pyridin-2-yl- and 4,6-dimethylpyrimidin-2-yl-cyanamides entered into an alkylation reaction in the form of sodium salts. Pyridin-2-yl cyanamide 2 was alkylated at endo-nitrogen atom of pyridine ring, while 4,6-dimethylpyrimidin-2-yl cyanamide 1 was effect

Ylide-induced ylide formation: A novel double cycloaddition reaction of a [1,2,4]triazolo[1,5-a]pyrimidinium ylides

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THERMOLYSIS OF TRIAZOLOL PYRIMIDINE N-YLIDES

5,7-Dimethyltriazolopyrimidinio-3-phenacylide (3) generated by the reaction of an iminium salt (2) with 1 eq. of triethylamine, underwent a new thermal ring cleavage of the triazole moiety to give the pyrimidine derivative.However reaction o