16973-99-2

Basic information

• Product Name: 4-Pyrimidinamine, N-(phenylmethyl)-
• CAS NO: 16973-99-2
• Molecular Formula: C11H11N3
• Molecular Weight: 185.228
• Mol File: 16973-99-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4-Pyrimidinamine, N-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Pyrimidinamine, N-(phenylmethyl)-(16973-99-2)
• EPA Substance Registry System: 4-Pyrimidinamine, N-(phenylmethyl)-(16973-99-2)

Safety Data

• Hazardous Substances Data: 16973-99-2(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 163133-86-6 pyrimidin-4-amine 
• 100-51-6 benzyl alcohol 
• 91719-61-8 N-benzyl-2-(methylthio)pyrimidin-4-amine 
• 100-46-9 benzylamine 
• 90042-88-9 4-benzilamino-2,6-tricloropirimidina 

Relevant articles and documents

Reductive Amination Revisited: Reduction of Aldimines with Trichlorosilane Catalyzed by Dimethylformamide─Functional Group Tolerance, Scope, and Limitations

Aldimines, generated in situ from aliphatic, aromatic, and heteroaromatic aldehydes and aliphatic, aromatic, and heteroaromatic primary or secondary amines, can be reduced with trichlorosilane in the presence of dimethylformamide (DMF) as an organocatalys

A method for the reductive scission of heterocyclic thioethers

A mild, chemoselective, and generally high-yielding method for the reductive scission of heterocyclic thioethers is described. Suitable heterocycles have a thioether substituent at the 2-position relative to a ring heteroatom. The convenient and straightforward method is demonstrated with reactants which are not compatible with the standard Raney nickel conditions such as sulfides, sulfones, and thiophenes. In addition, benzyl esters, benzyl amides, and benzyl carbamates are tolerated by the reductive reaction conditions.