31408-23-8

Basic information

• Product Name: 2-Pyrimidinamine, 5-phenyl- (9CI)
• Synonyms: 2-Pyrimidinamine, 5-phenyl- (9CI);5-phenylpyriMidin-2-aMine
• CAS NO: 31408-23-8
• Molecular Formula: C₁₀H₉N₃
• Molecular Weight: 171.19856
• Product Categories: QUINAZOLINE;PYRIMIDINE
• Mol File: 31408-23-8.mol
• Article Data: 16

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Pyrimidinamine, 5-phenyl- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Pyrimidinamine, 5-phenyl- (9CI)(31408-23-8)
• EPA Substance Registry System: 2-Pyrimidinamine, 5-phenyl- (9CI)(31408-23-8)

Safety Data

• Hazardous Substances Data: 31408-23-8(Hazardous Substances Data)

Upstream product

• 86139-82-4 methoxy-3 phenyl-2 propenal 
• 113-00-8 guanidine nitrate 
• 4432-64-8 hydroxymethylenephenylacetaldehyde 
• 7752-82-1 5-bromo-2-aminopyrimidine 
• 98-80-6 phenylboronic acid 
• 119072-55-8 tert-butylisonitrile 
• 50-01-1 guanidine hydrochloride 
• 536-74-3 phenylacetylene 
• 108-86-1 bromobenzene 
• 936250-22-5 (2-aminopyrimidin-5-yl)boronic acid 
• 591-50-4 iodobenzene 
• 402960-38-7 5-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)pyrimidin-2-ylamine 
• 29110-75-6 N'-tosyl phenylhydrazine 
• 5905-69-1 1-bromo-4-(difluoromethoxy)benzene 

Downstream Products

• 201938-91-2 C₁₀H₇N₅O₄ 
• 78533-68-3 2-amino-5-phenyl-1,4,5,6-tetrahydropyrimidine 
• 85658-61-3 2-chloro-5-phenylpyrimidine 1-oxide 
• 726138-32-5 2-(4-bromo-phenyl)-6-phenyl-imidazo[1,2-a]pyrimidine 
• 328232-76-4 trans-3-oxo-N-(5-phenylpyrimidin-2-yl)-3H-spiro[6-aza-2-benzofuran-1,1'-cyclohexane]-4'-carboxamide 
• 328232-54-8 trans-3-oxo-N-(5-phenylpyrimidin-2-yl)-3H-spiro[4-aza-2-benzofuran-1,1'-cyclohexane]-4'-carboxamide 
• 328232-63-9 trans-3-oxo-N-(5-phenylpyrimidin-2-yl)-3H-spiro[5-aza-2-benzofuran-1,1'-cyclohexane]-4'-carboxamide 
• 1192312-63-2 trans-3-oxo-N-(5-phenylpyrimidin-2-yl)-3H-spiro[7-aza-2-benzofuran-1,1'-cyclohexane]-4'-carboxamide 
• 328232-44-6 Trans-3'oxo-N-(5-phenyl-2-pyrimidinyl)spiro[cyclohexane-1,1'(3'H)-isobenzofuran]-4-carboxamide 
• 1380235-02-8 N-butyl-5-phenylpyrimidin-2-amine 

Relevant articles and documents

Asymmetric pyrene derivatives comprising amine group including heteroaryl group and organic light-emitting diode including the same

The present invention relates to a pyrene derivative represented by [chemical formula A] or [chemical formula B], and an organic light emitting diode comprising the same, wherein substituents Py_1, Py_2, Ar_1, Ar_2, Z, and m are defined in the detailed de

Probing the Scope of the Amidine–1,2,3-triazine Cycloaddition as a Prospective Click Ligation Method

Despite recent achievements in the development of chemical reactions enabling selective modification of complex biomolecules, the demand for fast and efficient methodologies that allow the attachment of various functional groups to these systems is the subject of intense research. Here, we report on the study of the amidine–1,2,3-triazine cycloaddition reaction, which has the potential to address many of the challenges associated with the development of such chemistry. We describe an optimized protocol leading to the in situ formation of free amidine bases, which directly react in the cycloaddition reaction with 1,2,3-triazines. Our kinetic studies reveal the structural features determining the reaction rates. Finally, we show that the amidine–1,2,3-triazine cycloaddition is extraordinarily selective and orthogonal to other popular ligation reactions. The pros and cons of the methodology are presented.

The Dimroth rearrangement as a probable cause for structural misassignments in imidazo[1,2-a]pyrimidines: A 15N-labelling study and an easy method for the determination of regiochemistry

Structural misassignments are often seen for complex natural products, but this can also be an issue with seemingly simpler structures. In this paper, we describe how, using a 15N-labelled analogue, we established that the Dimroth rearrangement