35782-30-0

Basic information

• Product Name: Pyrimidine, 2-[(1E)-2-phenylethenyl]- (9CI)
• Synonyms: Pyrimidine, 2-[(1E)-2-phenylethenyl]- (9CI)
• CAS NO: 35782-30-0
• Molecular Formula: C₁₂H₁₀N₂
• Molecular Weight: 182.2212
• Product Categories: PYRIMIDINE
• Mol File: 35782-30-0.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Pyrimidine, 2-[(1E)-2-phenylethenyl]- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Pyrimidine, 2-[(1E)-2-phenylethenyl]- (9CI)(35782-30-0)
• EPA Substance Registry System: Pyrimidine, 2-[(1E)-2-phenylethenyl]- (9CI)(35782-30-0)

Safety Data

• Hazardous Substances Data: 35782-30-0(Hazardous Substances Data)

Upstream product

• 5053-43-0 2-methylpyrimidine 
• 100-52-7 benzaldehyde 
• 103-64-0 bromostyrene 
• 153435-63-3 2-(tributylstannyl)pyrimidine 
• 66680-87-3 (E)-1-phenyl-(2-tributylstannyl)ethene 
• 154447-06-0 2-pyrimidinyl triflate 
• 1722-12-9 2-chloropyrimidine 
• 6783-05-7 trans-2-phenylvinylboronic acid 
• 1780-26-3 2,4-dichloro-2-methylpyrimidine 
• 4595-60-2 2-bromopyrimidine 
• 1305318-31-3 2-phenethylpyrimidine 
• 100-51-6 benzyl alcohol 

Downstream Products

• 31519-62-7 pyrimidine-2-carboxylic acid 

Relevant articles and documents

The facile route to stereodefined alkenyl-substituted pyrimidines

The Suzuki-Miyaura type cross-coupling reactions of various chloropyrimidines with Stereodefined alkenylboronic acids giving the corresponding alkenyl-substituted pyrimidines were studied. The experiments discovered that the reaction is stereospecific and

Aryl-Nickel-Catalyzed Benzylic Dehydrogenation of Electron-Deficient Heteroarenes

This manuscript describes the first practical benzylic dehydrogenation of electron-deficient heteroarenes, including pyridines, pyrazines, pyrimidines, pyridazines, and triazines. This transformation allows for the efficient benzylic oxidation of heteroarenes to afford heterocyclic styrenes by the action of nickel catalysis paired with an unconventional bromothiophene oxidant.

SYNTHESIS OF PYRIMIDINYL TRIFLATES AND PALLADIUM-CATALYZED COUPLING WITH ORGANOTIN AND ORGANOZINC REAGENTS

Pyrimidinyl triflates have been synthesized from pyrimidinones using triflic anhydride in the presence of triethylamine.The triflates, in the pyrimidine electrophilic positions, are versatile intermediates for substitution reactions.Carbon substituents ar