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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.

907594-98-3

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907594-98-3 Usage

Uses

Used in Organic Chemistry:
2-Pyrimidinemethanamine, -alpha--phenyl(9CI) is used as a building block for the synthesis of various organic compounds. Its unique structure and reactivity make it a valuable component in the development of new organic molecules.
Used in Pharmaceutical Synthesis:
2-Pyrimidinemethanamine, -alpha--phenyl(9CI) is used as a building block in the synthesis of various pharmaceuticals and agrochemicals. Its structural similarity to other biologically active molecules makes it a promising candidate for the development of new drugs and agrochemicals.
Used in Research:
2-Pyrimidinemethanamine, -alpha--phenyl(9CI) is used in research to study its pharmacological properties and potential biological activities. Further research is needed to fully understand and utilize the potential applications of 2-Pyrimidinemethanamine, -alpha--phenyl- (9CI) in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 907594-98-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,7,5,9 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 907594-98:
(8*9)+(7*0)+(6*7)+(5*5)+(4*9)+(3*4)+(2*9)+(1*8)=213
213 % 10 = 3
So 907594-98-3 is a valid CAS Registry Number.

907594-98-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name phenyl(pyrimidin-2-yl)methanamine

1.2 Other means of identification

Product number -
Other names 2-pyrimidylphenylmethylamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:907594-98-3 SDS

907594-98-3Relevant academic research and scientific papers

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

Grach, Guillaume,Pieters, Gregory,Dinut, Aurelia,Terrasson, Vincent,Medimagh, Raouf,Bridoux, Alexandre,Razafimahaleo, Vanessa,Gaucher, Anne,Marque, Sylvain,Marrot, Jerome,Prim, Damien,Gil, Richard,Planas, Jose Giner,Vinas, Clara,Thomas, Isabelle,Roblin, Jean-Philippe,Troin, Yves

scheme or table, p. 4074 - 4086 (2011/10/03)

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%.

N-heterocyclic benzhydrylamines as new N,N-bidentate ligands in palladium complexes: Synthesis, characterization and catalytic activity

Terrasson, Vincent,Prim, Damien,Marrot, Jerome

experimental part, p. 2739 - 2745 (2009/03/12)

The synthesis of new N,N-bidentate ligands based on a π-deficient N-heterocyclic benzhydrylamine core is described. The corresponding air-stable palladium complexes are obtained in high yields and fully characterized by NMR spectroscopy and X-ray structur

Synthesis of homo- and heterobiarylmethylamines

Terrasson, Vincent,Marque, Sylvain,Scarpacci, Annabelle,Prim, Damien

, p. 1858 - 1862 (2008/01/27)

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

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