17759-27-2

Basic information

• Product Name: 4-Methyl-6-phenylpyrimidine
• Synonyms: 4-Methyl-6-phenylpyrimidine
• CAS NO: 17759-27-2
• Molecular Formula: C₁₁H₁₀N₂
• Molecular Weight: 170.21
• Mol File: 17759-27-2.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-Methyl-6-phenylpyrimidine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Methyl-6-phenylpyrimidine(17759-27-2)
• EPA Substance Registry System: 4-Methyl-6-phenylpyrimidine(17759-27-2)

Safety Data

• Hazardous Substances Data: 17759-27-2(Hazardous Substances Data)

Upstream product

• 77287-34-4 formamide 
• 93-91-4 1-phenylbutan-1,3-dione 
• 3435-25-4 4-methyl-6-chloropyrimidine 
• 98-80-6 phenylboronic acid 
• 3438-55-9 5-bromo-4-chloro-6-methylpyrimidine 
• 463-52-5 formamidine 
• 64-17-5 ethanol 
• 91021-28-2 4-phenyl-6-trichloromethylpyrimidine 
• 32785-40-3 2-chloro-4-phenyl-6-methylpyrimidine 
• 40808-16-0 4-chloro-4-phenyl-but-3-en-2-one 
• 27955-44-8 4-methyl-6-phenylpyrimidine-2(1H)-thione 
• 3438-46-8 4-Methylpyrimidine 

Downstream Products

• 28840-36-0 6-phenylpyrimidine-4-carboxamide 
• 74647-38-4 6-phenylpyrimidine-4-carboxylic acid methyl ester 
• 74502-99-1 N-methyl-6-phenylpyrimidine-4-carboxamide 
• 74647-32-8 ethyl 6-phenylpyrimidine-4-carboxylate 
• 74503-00-7 N,N-dimethyl-6-phenylpyrimidine-4-carboxamide 
• 74502-98-0 (6-phenylpyrimidin-4-yl)methanol 
• 28668-32-8 6-phenylpyrimidine-4-carboxylic acid 
• 73937-26-5 4-methyl-6-phenylpyrimidine-2-carboxamide 
• 64571-52-4 2,5-diacetyl-4-methyl-6-phenylpyrimidine 
• 64571-48-8 2-acetyl-4-methyl-6-phenylpyrimidine 
• 76132-95-1 4-phenyl-6-(2-piperidinoethyl)pyrimidine 
• 76132-97-3 4-phenyl-6-(1-piperidinomethylvinyl)pyrimidine 
• 76132-93-9 4-phenyl-6-bis(piperidinomethyl)methylpyrimidine 
• 17759-10-3 4-methyl-6-phenyl-pyrimidine-1-oxide 

Relevant articles and documents

ORGANOMETALLIC COMPLEX, LIGHT-EMITTING ELEMENT, LIGHT-EMITTING DEVICE, ELECTRONIC DEVICE, AND LIGHTING DEVICE

To provide a novel organometallic complex. The organometallic complex is represented by Formula (G1) and includes a central metal, a first ligand, and a second ligand. The first ligand and the second ligand are cyclometalated ligands. At least one of the

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Provided is a novel heterocyclic compound which can be used in a light-emitting layer of a light-emitting element as a host material in which a light-emitting substance is dispersed. A heterocyclic compound represented by a general formula (G1) is provide

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Provided is a novel heterocyclic compound which can be used in a light-emitting layer of a light-emitting element as a host material in which a light-emitting material is dispersed, i.e., a heterocyclic compound represented by a general formula (G1). Any one of R1 to R10 represents a substituent represented by a general formula (G1-1); another one of R1 to R10 represents hydrogen, an alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, or a substituent represented by a general formula (G1-2); and the others separately represent hydrogen, an alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted phenyl group, or a substituted or unsubstituted biphenyl group.

ORGANOMETALLIC COMPLEX, LIGHT-EMITTING ELEMENT, LIGHT-EMITTING DEVICE, ELECTRONIC DEVICE AND LIGHTING DEVICE

Provided is a novel substance that can emit phosphorescence. Alternatively, provided is a novel substance with high emission efficiency. An organometallic complex in which a 4-arylpyrimidine derivative is a ligand and iridium is a central metal is provided. Specifically, an organometallic complex having a structure represented by a general formula (G1) is provided. In the general formula (G1), R1 represents a substituted or unsubstituted alkyl group having 1 to 4 carbon atoms or a substituted or unsubstituted aryl group having 6 to 10 carbon atoms, R2 represents any of hydrogen, a substituted or unsubstituted alkyl group having 1 to 4 carbon atoms, and a substituted or unsubstituted phenyl group, R3 represents hydrogen or a substituted or unsubstituted alkyl group having 1 to 4 carbon atoms, and Ar1 represents a substituted or unsubstituted arylene group having 6 to 10 carbon atoms.

HETEROCYCLIC COMPOUND

Provided is a novel heterocyclic compound which can be used for a light-emitting element, as a host material of a light-emitting layer in which a light-emitting substance is dispersed. A heterocyclic compound represented by a general formula (G1) is provi

Light-Emitting Device, Electronic Device, and Lighting Device Utilizing Phosphorescence

A new light-emitting device utilizing phosphorescence is provided. Further, an electronic device and a lighting device which utilize phosphorescence are provided. One embodiment of the present invention is a light-emitting device including a phosphorescen

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.

Suzuki-Miyaura and Negishi approaches to a series of forensically relevant pyridines and pyrimidines

A library of 5-aryl-4-methylpyrimidines, phenyl ring-substituted derivatives of 4-benzylpyrimidines, 2,6-benzylpyridines, and 2,6-dibenzyl-4-methylpyridines were prepared. The synthesis of 5-aryl-4-methylpyrimidines was accomplished by Suzuki-Miyaura cross-coupling reaction between arylboronic acids and 5-bromo-4-methylpyrimidine. The 4-benzylpyrimidines and 2,6-benzylpyridines were synthesized by treatment of 4-bromopyrimidine and 2,6-dibromopyridine derivatives with ring-substituted benzylzinc reagents. Georg Thieme Verlag Stuttgart.

REDUCTIVE FORMATION OF PYRIMIDINYLMETHYLENEPHOSPHORANES BY REACTION OF TRICHLOROMETHYLPYRIMIDINES WITH TRIPHENYLPHOSPHINE

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