17749-82-5

Basic information

• Product Name: Pyrimidine, 4-(2-furanyl)- (9CI)
• Synonyms: Pyrimidine, 4-(2-furanyl)- (9CI)
• CAS NO: 17749-82-5
• Molecular Formula: C₈H₆N₂O
• Molecular Weight: 146.14604
• Product Categories: PYRIMIDINE
• Mol File: 17749-82-5.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Pyrimidine, 4-(2-furanyl)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Pyrimidine, 4-(2-furanyl)- (9CI)(17749-82-5)
• EPA Substance Registry System: Pyrimidine, 4-(2-furanyl)- (9CI)(17749-82-5)

Safety Data

• Hazardous Substances Data: 17749-82-5(Hazardous Substances Data)

Upstream product

• 110-00-9 furan 
• 289-95-2 PYRIMIDINE 
• 2786-02-9 2-lithiofuran 
• 60-29-7 diethyl ether 
• 1192-62-7 1-(2-furyl)-1-ethanone 
• 6966-73-0 triformylaminomethane 
• 77287-34-4 formamide 
• 3473-63-0 formamidine acetic acid 
• 17168-45-5 3-(dimethylamino)-1-(furan-2-yl)-2-propen-1-one 
• 290-87-9 1,3,5-Triazine 
• 17758-33-7 3-methyl-5-nitro-4(3H)-pyrimidinone 

Downstream Products

• 883829-10-5 C₂₂H₁₅F₃N₂O₄ 
• 883829-13-8 C₂₂H₁₅F₃N₂O₄ 
• 883823-18-5 C₂₁H₁₅BrN₂O₄ 

Relevant articles and documents

Synthesis of a novel bipyrimidine dicarboxylic acid ligand for the preparation of panchromatic ruthenium dyes

A novel ruthenium complex with a new 4,4′-bipyrimidine-6,6′-dicarboxylic acid ligand (H2dcbpm) has been synthesized and its properties were investigated for application in dye-sensitized solar cells. The new dye shows a wide range of absorption of the solar spectrum with maximum of absorption at 665 nm corresponding to a 100 nm redshift compared to the precursor complex ([Ru(dcbpyH2)2(Cl)2]) of the commercial N719 dye. The energies of HOMO-LUMO obtained by voltammetry and DFT calculations show an overall stabilization of the orbitals of the bipyrimidine complex compared to the bipyridine one. Despite having promising absorption properties, the redox potentials of this complex make it unsuitable for charge injection into the conduction band on TiO2. Nevertheless, the newly prepared ligand provides an additional tuning path to adjust the energy levels of the complex in order to benefit from the red-shifted absorption it offers.

Fast and green one-pot multicomponent synthesis of a library of pyrrolo[1,2-c] pyrimidines under microwave irradiation

A simple, clean and rapid one-pot three component, microwave-assisted synthesis of pyrrolo[1,2-c]pyrimidine derivatives starting from various substituted pyrimidines, 2-bromoacetophenones and nonsymmetrical, electron deficient alkynes in 1,2-epoxybutane which acts both as solvent and acid scavenger is reported. This one-pot three component synthesis implies short reaction times being at the same time highly cost-effective and environmental friendly.

Novel synthesis of bihetaryl compounds

The ring transformation of nitropyrimidinone 1 with acetophenone derivatives 2 affords two kinds of azaheterocyclic compounds, 4-phenylpyrimidines 3 and 3-nitro-6-phenyl-2-pyridones 4. On the basis of the relationship between electronic properties of the substituent and ratios of products, a plausible reaction mechanism is provided. Furthermore, the present reaction could be applied to heterocyclic ketones giving bihetaryl compounds.