174303-49-2

Basic information

• Product Name: Pyrimidine, 2,2-(1,4-phenylene)bis- (9CI)
• Synonyms: Pyrimidine, 2,2-(1,4-phenylene)bis- (9CI)
• CAS NO: 174303-49-2
• Molecular Formula: C₁₄H₁₀N₄
• Molecular Weight: 234.256
• Product Categories: QUINAZOLINE;PYRIMIDINE
• Mol File: 174303-49-2.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Pyrimidine, 2,2-(1,4-phenylene)bis- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Pyrimidine, 2,2-(1,4-phenylene)bis- (9CI)(174303-49-2)
• EPA Substance Registry System: Pyrimidine, 2,2-(1,4-phenylene)bis- (9CI)(174303-49-2)

Safety Data

• Hazardous Substances Data: 174303-49-2(Hazardous Substances Data)

Upstream product

• 1722-12-9 2-chloropyrimidine 
• 106-37-6 1.4-dibromobenzene 
• 4612-26-4 1,4-Phenyldiboronic acid 
• 4595-60-2 2-bromopyrimidine 

Relevant articles and documents

Ruthenium(II)-Catalyzed Microwave-Promoted Multiple C-H Activation in Synthesis of Hexa(heteroaryl)benzenes in Water

A series of hexa(heteroaryl)benzenes were synthesized by the Ru(II)-carboxylate-catalyzed multiple C-H activation of benzenes carrying pyridyl, pyrimidyl, or pyrazolyl directing groups using N-heteroaryl bromides as coupling partners. The reactions procee

Cobalt-catalyzed cross-coupling between in situ prepared arylzinc halides and 2-chloropyrimidine or 2-chloropyrazine

A cobalt-catalyzed cross-coupling of aryl halides with 2-chloropyrimidines or 2-chloropyrazines is reported in satisfactory to high yields. The key step of this procedure is the formation of aromatic organozinc reagents and their coupling with 2-chlorodia

Synthesis of oligo(diazaphenyls). Tailor-made fluorescent heteroaromatics and pathways to nanostructures

Oligoaza derivatives of biphenyl, terphenyl, quaterphenyl, quinquephenyl, sexiphenyl, septiphenyl, octiphenyl, noviphenyl, deciphenyl and dodeciphenyl and poly(pyrimidinylenephenylene) can be synthesized from readily accessible vinamidinium salts and amidines or N,N,N'- tris(trimethylsilyl)amidines. The fluorescence of these systems can be tuned over a wide spectral range by varying number and positions of N atoms. Oligo(diazaphenyls) are thermally and photochemically stable, are easier to reduce than oligopheny]s, can be dissolved at any rate in strong acids and show strong blue fluorescence in solution as well as in the solid state.