21203-79-2

Basic information

• Product Name: 2-METHYL-4-PHENYLPYRIMIDINE
• Synonyms: 2-METHYL-4-PHENYLPYRIMIDINE
• CAS NO: 21203-79-2
• Molecular Formula: C₁₁H₁₀N₂
• Molecular Weight: 170.21
• Mol File: 21203-79-2.mol
• Article Data: 15

Chemical Properties

• Melting Point: 54-55 °C
• Boiling Point: 291.8±9.0 °C(Predicted)
• Appearance: /
• Density: 1.081±0.06 g/cm3(Predicted)
• PKA: 1.93±0.20(Predicted)
• CAS DataBase Reference: 2-METHYL-4-PHENYLPYRIMIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-METHYL-4-PHENYLPYRIMIDINE(21203-79-2)
• EPA Substance Registry System: 2-METHYL-4-PHENYLPYRIMIDINE(21203-79-2)

Safety Data

• Hazardous Substances Data: 21203-79-2(Hazardous Substances Data)

Usage

General Description

2-Methyl-4-phenylpyrimidine is a chemical compound with the molecular formula C12H10N2. It is a pyrimidine derivative, consisting of a pyrimidine ring with a methyl and a phenyl group attached to it. 2-METHYL-4-PHENYLPYRIMIDINE has potential applications in the field of pharmaceuticals, particularly in drug discovery and development. It is known to have biological activity and may possess pharmacological properties, making it a potential candidate for drug design and synthesis. Its specific uses and effects depend on the context in which it is applied, but its unique molecular structure and properties make it an interesting and potentially valuable chemical compound for various research and industrial applications.

Upstream product

• 124-42-5 acetamidine hydrochloride 
• 3623-15-2 phenyl propargyl ketone 
• 14804-59-2 3-bromo-3-phenylacrylaldehyde 
• 104-55-2 3-phenyl-propenal 
• 93-55-0 1-phenyl-propan-1-one 
• 1780-26-3 2,4-dichloro-2-methylpyrimidine 
• 98-80-6 phenylboronic acid 
• 13788-90-4 3,3-dimethoxy-1-phenylpropan-1-one 
• 100580-13-0 2-methyl-4-phenyl-3,4-dihydropyrimidine 
• 5053-43-0 2-methylpyrimidine 
• 1078-58-6 diphenylzinc 
• 66129-60-0 ethyl-3-(dimethylamino)-2-(phenylcarbonyl)prop-2-enoate 
• 127957-93-1 2-methyl-4-phenyl-pyrimidine-5-carboxylic acid ethyl ester 
• 99-90-1 para-bromoacetophenone 

Downstream Products

• 73937-28-7 4-benzoyl-2-methyl-6-phenylpyrimidine 
• 64571-46-6 methyl 2-methyl-6-phenyl-4-pyrimidinyl ketone 
• 73937-22-1 2-methyl-6-phenylpyrimidine-4-carboxamide 
• 73937-27-6 4-isobutyroyl-2-methyl-6-phenylpyrimidine 
• 13739-48-5 2-methyl-4-phenyl-imidazole 
• 65-85-0 benzoic acid 
• 69098-69-7 2-methyl-4-phenylpyrimidine 1-oxide 
• 74647-39-5 6-phenylpyrimidine-2-carboxylic acid 
• 74647-41-9 N,N-dimethyl-6-phenylpyrimidine-2-carboxamide 
• 76132-83-7 4-phenyl-2-styrylpyrimidine 1-oxide 
• 76132-84-8 2-(2-hydroxy-2-phenylethyl)-4-phenylpyrimidine 1-oxide 
• 74647-40-8 methyl 6-phenylpyrimidine-2-carboxylate 
• 73937-23-2 2-methyl-6-phenylpyrimidine-4-(N,N-dimethyl)carboxamide 
• 74502-90-2 ethyl 2-methyl-6-phenyl-4-pyrimidinyl ketone 

Relevant articles and documents

Au(I)-catalyzed domino intramolecular cyclization for the synthesis of 2,4-disubstituted pyrimidines

An efficient Au-catalyzed domino intramolecular cyclization reaction has been developed for the construction of pyrimidine derivatives from ynals and amidines at room temperature for 3 h. This transformation provides a new method for the formation of C-C

Heterogeneous gold(I)-catalyzed cyclization between ynals and amidines: An efficient and practical synthesis of 2,4-disubstituted pyrimidines

A novel and highly efficient heterogeneous gold(I)-catalyzed cyclization between ynals and amidines has been developed that proceeds smoothly under mild conditions and provides a general and practical method for the synthesis of a wide variety of 2,4-disu

Pyrimidine as an Aryl C-H Activating Group

The Pd-catalyzed regioselective C-H activation/arylation, /iodination, and/acetoxylation reactions of 4-arylpyrimidines using aryl iodides, N-iodosuccinimide, and (diacetoxyiodo)benzene respectively as coupling partners are described. Suzuki-Miyaura coupl

Transition Metal Free Intermolecular Direct Oxidative C-N Bond Formation to Polysubstituted Pyrimidines Using Molecular Oxygen as the Sole Oxidant

Various polysubstituted pyrimidines are smoothly formed via a base-promoted intermolecular oxidation C-N bond formation of allylic C(sp3)-H and vinylic C(sp2)-H of allyllic compounds with amidines using O2 as the sole oxid