16133-83-8

Basic information

• Product Name: 2-phenyl-tetrahydrofuran
• Synonyms: 2-phenyl-tetrahydrofuran;2-phenyloxolane
• CAS NO: 16133-83-8
• Molecular Formula: C₁₀H₁₂O
• Molecular Weight: 148.20168
• Mol File: 16133-83-8.mol
• Article Data: 79

Chemical Properties

• Melting Point: 91-92 °C
• Boiling Point: 105 °C(Press: 14 Torr)
• Appearance: /
• Density: 1.037 g/cm3(Temp: 15 °C)
• CAS DataBase Reference: 2-phenyl-tetrahydrofuran(CAS DataBase Reference)
• NIST Chemistry Reference: 2-phenyl-tetrahydrofuran(16133-83-8)
• EPA Substance Registry System: 2-phenyl-tetrahydrofuran(16133-83-8)

Safety Data

• Hazardous Substances Data: 16133-83-8(Hazardous Substances Data)

Usage

General Description

2-phenyl-tetrahydrofuran, also known as PT, is a chemical compound with the formula C10H12O. It is a colorless liquid that is insoluble in water but soluble in organic solvents. PT is used as a solvent and intermediate in the synthesis of pharmaceuticals and other organic compounds. It can also be found in some consumer products such as perfumes and cosmetics. PT has been found to have potential applications in the production of bio-based fuels and renewable chemicals due to its unique structure and properties. However, it is important to handle PT with care as it can be harmful if ingested or inhaled, and it may cause skin and eye irritation upon contact.

Upstream product

• 770-36-5 4-phenylbuta-3-en-1-ol 
• 503-30-0 trimethylene oxide 
• 67-56-1 methanol 
• 908094-04-2 phenyldiazomethane 
• 1191-99-7 2,3-dihydro-2H-furan 
• 108-86-1 bromobenzene 
• 120346-80-7 tetrahydro-2-(phenylsulphonyl)furan 
• 3360-41-6 4-phenyl-butan-1-ol 
• 4850-50-4 1-phenyl-butane-1,4-diol 
• 36866-66-7 5-phenyloxolan-2-ol 
• 124468-98-0 4-trimethylsiloxybutyrophenone 
• 100-52-7 benzaldehyde 
• 1073-05-8 1,3,2-dioxathiane 2,2-dioxide 
• 591-50-4 iodobenzene 

Downstream Products

• 74-85-1 ethene 
• 1636-34-6 2,3-diphenyl-2,3-butanediol 
• 98-85-1 1-Phenylethanol 
• 98-86-2 acetophenone 
• 7515-42-6 (3E)-4-phenylbut-3-en-1-yl acetate 
• 3360-41-6 4-phenyl-butan-1-ol 
• 107686-18-0 4-Phenyl-hept-5-yn-1-ol 
• 107686-17-9 1-ethenyl-(4-hydroxy-1-phenyl-1-butyl)cyclohexane 
• 107686-16-8 4-phenyl-6-heptene-1-ol 
• 71052-93-2 1-phenyl-1,4-dibromobutane 
• 87372-61-0 2-phenyl-2-allyltetrahydrofuran 
• 1469994-83-9 trimethyl(2-phenyltetrahydrofuran-2-yl)silane 
• 1469994-84-0 2-phenyl-2-(tributylstannyl)tetrahydrofuran 
• 1469994-85-1 2-phenyl-2-(phenylthio)tetrahydrofuran 

Relevant articles and documents

Oxidation of Unsaturated Aliphatic and Arylalkyl Alcohols by Peroxydisulphate. Intramolecular Cyclization of Alkoxyl Radicals

Oxidation of unsaturated aliphatic and arylalkyl alcohols by the sodium peroxydisulphate-silver salt system has benn studied.Both classes of alcohols lead to cyclic ethers through different pathways.The ratio of five- to six-membered cyclic ethers was est

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C1-Symmetric Binap Derivative Featuring Single Diferrocenylphosphino-Donor Moiety

A C1-symmetric chiral bisphosphine, FcPh-Binap (1), which possesses a single diferrocenylphosphino moiety together with a conventional Ph2P-substituent, was prepared in enantiomerically pure forms. Ligand 1 is sterically less demanding than Fc-Segphos (A)

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