907594-98-3

Basic information

• Product Name: 2-Pyrimidinemethanamine, -alpha--phenyl- (9CI)
• Synonyms: 2-Pyrimidinemethanamine, -alpha--phenyl- (9CI);Phenyl(pyrimidin-2-yl)methanamine
• CAS NO: 907594-98-3
• Molecular Formula: C₁₁H₁₁N₃
• Molecular Weight: 185.22514
• Product Categories: QUINAZOLINE;PYRIMIDINE
• Mol File: 907594-98-3.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-Pyrimidinemethanamine, -alpha--phenyl- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Pyrimidinemethanamine, -alpha--phenyl- (9CI)(907594-98-3)
• EPA Substance Registry System: 2-Pyrimidinemethanamine, -alpha--phenyl- (9CI)(907594-98-3)

Safety Data

• Hazardous Substances Data: 907594-98-3(Hazardous Substances Data)

Usage

General Description

2-Pyrimidinemethanamine, -alpha--phenyl- (9CI) is a chemical compound with the molecular formula C10H9N3. It is a derivative of pyrimidine with a phenyl group attached to the alpha carbon. 2-Pyrimidinemethanamine, -alpha--phenyl- (9CI) has potential applications in organic chemistry and pharmaceutical synthesis due to its unique structure and reactivity. It may be used as a building block in the synthesis of various pharmaceuticals and agrochemicals. Additionally, research on the pharmacological properties and potential biological activities of this compound may also be of interest, given its structural similarity to other biologically active molecules. However, further research is needed to fully understand and utilize the potential applications of 2-Pyrimidinemethanamine, -alpha--phenyl- (9CI) in various fields.

Upstream product

• 100-47-0 benzonitrile 
• 14080-23-0 2-cyanopyrimidine 
• 100-59-4 phenylmagnesium chloride 

Downstream Products

• 1161432-26-3 N-benzyl-N-[phenyl(pyrimidin-2-yl)methyl]amine 
• 1089664-81-2 C₂₀H₁₇FN₄O₂ 

Relevant articles and documents

N-heterocyclic pyridylmethylamines: Synthesis, complexation, molecular structure, and application to asymmetric Suzuki-Miyaura and oxidative coupling reactions

The synthesis of N,N-bidentate ligands based on a π-deficient N-heterocyclic pyridylmethylamine core is described. The preparation and characterization of the corresponding N,N-ligand-palladium complexes in solution and the solid state are illustrated. Pd complexes showed a good yield and moderate catalytic activity (up to 40% ee) in the asymmetric Suzuki-Miyaura coupling reaction, leading to methoxybinaphthyl derivatives. The combination of N,N-pyridylmethylamines with cuprous iodide revealed effective catalytic systems in oxidative naphthol derivative coupling reactions, affording the corresponding binaphthyls in high yields and with enantioselectivities of up to 61%.

Synthesis of homo- and heterobiarylmethylamines

A variety of homo- and heterobiarylmethylamines were prepared in modest to high yields via a convenient one-pot process. Georg Thieme Verlag Stuttgart.