112393-76-7

Basic information

• Product Name: ethyl-α-cyano-6-methyl-3-phenyl-as-triazine-5-acetate
• CAS NO: 112393-76-7
• Molecular Weight: 282.302
• Mol File: 112393-76-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: ethyl-α-cyano-6-methyl-3-phenyl-as-triazine-5-acetate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl-α-cyano-6-methyl-3-phenyl-as-triazine-5-acetate(112393-76-7)
• EPA Substance Registry System: ethyl-α-cyano-6-methyl-3-phenyl-as-triazine-5-acetate(112393-76-7)

Safety Data

• Hazardous Substances Data: 112393-76-7(Hazardous Substances Data)

Upstream product

• 107126-31-8 6-methyl-3-phenyl-2,5-dihydro-as-triazine-5-sulfonic acid monohydrate 
• 112393-75-6 6-methyl-3-phenyl-2,5-dihydro-as-triazine 
• 33449-34-2 6-methyl-5-oxo-3-phenyl-2,5-dihydro-as-triazine 
• 37967-82-1 6-methyl-3-phenyl-1,2,4-triazine 
• 94398-25-1 5-chloro-6-methyl-3-phenyl-2,5-dihydro-as-triazine 
• 105-56-6 ethyl 2-cyanoacetate 
• 54673-31-3 5-methoxy-6-methyl-3-phenyl-[1,2,4]triazine 

Relevant articles and documents

REACTION OF METHOXY-N-HETEROAROMATICS WITH PHENYLACETONITRILE UNDER BASIC CONDITIONS

The monomethoxyl derivatives of various ?-electron deficient N-heteroaromatics reacted with phenylacetonitrile in tetrahydrofuran in the presence of sodium hydride to give α-phenyl-N-heteroareneacetonitriles in the yields ranging from 45 to 78percent.On the contrary, the reaction of these methoxyl derivatives with ethyl cyanoacetate or malononitrile under similar conditions was restricted within narrow limits.The synthesis of benzoyl-N-heteroaromatics by the air-oxidation of α-phenyl-N-hetroareneacetonitriles was described additionally.

STUDIES ON AS-TRIAZINE DERIVATIVES. IX. SYNTHESIS OF 5-SUBSTITUTED 1,2,4-TRIAZINE DERIVATIVES THROUGH AN ADDITION REACTION AND SUBSEQUENT OXIDATION

The addition reactions of various nucleophiles to 6-methyl-3-phenyl-1,2,4-triazine (1) were investigated and a practical preparation of 1 was developed.The reactions showed many similarities to those of quinazoline (at the 4-position) and acridine (at the