27110-82-3

Basic information

• Product Name: Pyrimidine, 2-(2-furanyl)- (9CI)
• Synonyms: Pyrimidine, 2-(2-furanyl)- (9CI)
• CAS NO: 27110-82-3
• Molecular Formula: C8H6N2O
• Molecular Weight: 146.14604
• Product Categories: PYRIMIDINE
• Mol File: 27110-82-3.mol
• Article Data: 6

Chemical Properties

• Melting Point: 67-69 °C
• Boiling Point: 154.5±22.0 °C(Predicted)
• Appearance: /
• Density: 1.179±0.06 g/cm3(Predicted)
• PKA: 1.10±0.13(Predicted)
• CAS DataBase Reference: Pyrimidine, 2-(2-furanyl)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Pyrimidine, 2-(2-furanyl)- (9CI)(27110-82-3)
• EPA Substance Registry System: Pyrimidine, 2-(2-furanyl)- (9CI)(27110-82-3)

Safety Data

• Hazardous Substances Data: 27110-82-3(Hazardous Substances Data)

Upstream product

• 118486-94-5 2-(tributylstannyl)furan 
• 14080-18-3 2-(pyrimidinylthio)benzene 
• 98-01-1 furfural 
• 1307747-65-4 C₈H₁₀N₂O 
• 1529529-43-8 C₁₅H₁₆N₂O₃S 
• 1450-85-7 2-thioxopyrimidine 
• 166328-14-9 potassium (furan-2-yl)trifluoroboranuide 
• 1722-12-9 2-chloropyrimidine 
• 823-09-6 2-(methylsulfanyl)pyrimidine 
• 54610-73-0 furan-5-carboxamidine 
• 927-63-9 3-dimethylaminoacrolein 
• 14189-82-3 3-(N-Methylanilino)-2-propenal 
• 54610-69-4 furan-2-carboxamidine hydrochloride 

Relevant articles and documents

Efficient and benign one-pot conversion of n-tosyl-1,4,5,6- tetrahydropyrimidines to pyrimidines via tandem β-elimination and aromatization

An efficient, mild, benign, and practical method for one-pot conversion of N-tosyl-1,4,5,6-tetrahydropyrimidines into pyrimidines is discussed in detail. In this method, N-tosyl-1,4,5,6-tetrahydropyrimidines are first prepared via N-tosylation of tetrahyd

Scope of the suzuki-Miyaura cross-coupling reactions of potassium heteroaryltrifluoroborates

A wide variety of bench-stable potassium heteroaryltrifluoroborates were prepared, and general reaction conditions were developed for their cross-coupling to aryl and heteroaryl halides. The cross-coupled products were obtained in good to excellent yields. This method represents an efficient and facile installation of heterocyclic building blocks onto preexisting organic substructures.

Copper(I)-promoted palladium-catalyzed cross-coupling of unsaturated tri-n-butylstannane with heteroaromatic thioether

(Matrix presented) Palladium-catalyzed cross-coupling of vinyl- and arylstannanes with π-electron-deficient heteroaromatics was performed in good yields. This Stille-type reaction was carried out with a methylthioether function as an electrophile in the presence of a copper(I) bromide-dimethyl sulfide complex.