17113-32-5

Basic information

• Product Name: 2-(4-METHYLPHENYL)FURAN
• Synonyms: 2-(4-METHYLPHENYL)FURAN;AKOS BAR-0985
• CAS NO: 17113-32-5
• Molecular Formula: C₁₁H₁₀O
• Molecular Weight: 158.2
• Mol File: 17113-32-5.mol
• Article Data: 57

Chemical Properties

• Boiling Point: 67-68 °C(Press: 0.8 Torr)
• Appearance: /
• Density: 1.028±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 2-(4-METHYLPHENYL)FURAN(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-METHYLPHENYL)FURAN(17113-32-5)
• EPA Substance Registry System: 2-(4-METHYLPHENYL)FURAN(17113-32-5)

Safety Data

• Hazardous Substances Data: 17113-32-5(Hazardous Substances Data)

Usage

Type of compound

Heterocyclic aromatic compound

Structural components

Furan ring, 4-methylphenyl group

Usage

Organic synthesis, pharmaceutical research (building block for various pharmaceuticals and bioactive compounds)

Biological activities

Antioxidant, anti-inflammatory properties

Potential risks

Mutagenic and genotoxic effects

Safety considerations

Careful handling and use in the laboratory

Upstream product

• 110-00-9 furan 
• 106-38-7 para-bromotoluene 
• 459-44-9 4-methylbenzenediazonium tetrafluoroborate 
• 106-49-0 p-toluidine 
• 584-12-3 2-bromofuran 
• 4294-57-9 para-methylphenylmagnesium bromide 
• 67-56-1 methanol 
• 14377-18-5 1-(4-methylphenyl)prop-2-yn-1-one 
• 6729-64-2 tri(p-tolyl)bismuth dichloride 
• 118486-94-5 2-(tributylstannyl)furan 
• 107536-32-3 tris(4-methylphenyl)bismuth diacetate 
• 617-90-3 2-furancarbonitrile 
• 6165-76-0 propargyl p-toluenesulfonate 
• 13331-23-2 fur-2-ylboronic acid 

Downstream Products

• 87689-43-8 bis(5-(p-tolyl)furan-2-yl)methane 
• 87689-39-2 Dimethyl-(5-p-tolyl-furan-2-ylmethyl)-amine; hydrochloride 
• 84185-77-3 (E)-2-(5-p-Tolyl-furan-2-yl)-but-2-enedioic acid 
• 84207-12-5 3-(p-tolyl)-6-hydroxyphthalic anhydride 
• 924635-61-0 4,5-dimethoxy-2-[5-(4-methylphenyl)-2-furyl(phenyl)methyl]-1-(4-methylphenylsulfonamido)benzene 
• 21053-98-5 5-(4-methylphenyl)-3H-furan-2-one 
• 69836-67-5 dimethyl 3-hydroxy-6-(4-methylphenyl)phthalate 
• 72310-68-0 2-(5-(p-tolyl)furan-2-yl)ethanol 

Relevant articles and documents

Pd-NHCs Enabled Suzuki-Miyaura Cross-Coupling of Arylhydrazines via C–N Bond Cleavage

We describe a highly efficient protocol for cross-coupling of phenylhydrazines with arylboronic acids by Pd-NHCs under aerobic reaction condition. A series of well-defined Pd-NHCs complexes were evaluated and the relationship between the structure and the catalytic properties was investigated. It was disclosed that the Pd-PEPPSI-IPr proved to be the robust precatalyst, providing access to a range of (hetero)biaryls in good to excellent yields.

Synthesis method of monosubstituted or disubstituted furan derivatives

The invention relates to the field of medicine synthesis, and provides a synthesis method of monosubstituted or disubstituted furan derivatives, wherein the synthesis method can be used for synthesizing various furan derivatives with different substituent groups and has high flexibility. According to the synthesis method of the monosubstituted or disubstituted furan derivatives, 5-hydroxymethyl-[delta]2-isoxazoline derivative is used as a raw material in an acidic solvent, and the monosubstituted or disubstituted furan derivatives are synthesized in one step under the action of a metal reducing agent; and according to the method, the furan derivatives with different substituent groups can be synthesized by adopting the 5-hydroxymethyl-[delta]2-isoxazoline derivatives with different substituent groups, high flexibility is achieved, the technical scheme is simple in step and mild in reaction condition, synthesis of the furan derivatives can be achieved through a one-pot method, the reaction yield is high, and large-scale production is facilitated.

ORGANIC SEMICONDUCTING MATERIAL AND ITS SYNTHESIS AND ORGANIC SEMICONDUCTING COMPONENT WITH THE MATERIAL

New absorbing materials of formula (I) for use in organic semiconducting components: