22078-90-6

Basic information

• Product Name: (5-PHENYL-FURAN-2-YL)-METHANOL
• Synonyms: (5-PHENYL-FURAN-2-YL)-METHANOL;(5-PHENYL-2-FURYL)METHANOL;AKOS BB-8303;ART-CHEM-BB B025316;ASISCHEM U67293;RARECHEM AL BD 0884;(5-phenyl-2-furyl)methanol(SALTDATA: FREE)
• CAS NO: 22078-90-6
• Molecular Formula: C₁₁H₁₀O₂
• Molecular Weight: 174.2
• Mol File: 22078-90-6.mol
• Article Data: 11

Chemical Properties

• Melting Point: 62.5-63 °C(Solv: benzene (71-43-2); hexane (110-54-3))
• Boiling Point: 302.6°C at 760 mmHg
• Flash Point: 136.8°C
• Appearance: /
• Density: 1.151g/cm³
• Vapor Pressure: 0.000433mmHg at 25°C
• Refractive Index: 1.569
• PKA: 13.95±0.10(Predicted)
• CAS DataBase Reference: (5-PHENYL-FURAN-2-YL)-METHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: (5-PHENYL-FURAN-2-YL)-METHANOL(22078-90-6)
• EPA Substance Registry System: (5-PHENYL-FURAN-2-YL)-METHANOL(22078-90-6)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• Hazardous Substances Data: 22078-90-6(Hazardous Substances Data)

Usage

General Description

(5-Phenyl-furan-2-yl)-methanol is a chemical compound with the molecular formula C11H10O2. It is an aromatic organic compound comprising a furan ring with a phenyl group attached to it, and a hydroxyl group. It is used in the synthesis of various pharmaceuticals and agrochemicals. It has potential applications as a building block in the production of other organic compounds. The compound is also known for its potential use in the development of new materials and as a starting material in the synthesis of biologically active compounds. However, further research is required to fully understand its potential applications and properties.

InChI:InChI=1/C11H10O2/c12-8-10-6-7-11(13-10)9-4-2-1-3-5-9/h1-7,12H,8H2

Upstream product

• 13803-39-9 5-phenylfuran-2-carbaldehyde 
• 98-00-0 (2-furyl)methyl alcohol 
• 108-90-7 chlorobenzene 
• 67-47-0 5-hydroxymethyl-2-furfuraldehyde 
• 57489-93-7 5-phenyl-2-furancarbonyl chloride 
• 88-14-2 2-furanoic acid 
• 62-53-3 aniline 
• 536-74-3 phenylacetylene 
• 56-82-6 Glyceraldehyde 
• 27230-58-6 (5-bromo-2-furan-2-yl)methanol 
• 98-80-6 phenylboronic acid 
• 585-70-6 5-bromo-furan-2-carboxylic acid 
• 1899-24-7 5-bromo-2-furancarboxaldehyde 
• 960-16-7 tributylphenylstannane 

Downstream Products

• 69914-23-4 2-Hydroxymethyl-5-phenyltetrahydrofuran 
• 216086-64-5 4-(5-phenylfur-2-ylmethyloxymethyl)-2-(2-methylphenyl)benzoic acid methyl ester 
• 533934-24-6 2-(5-phenyl)furylmethyl propargyl ether 
• 55181-88-9 2-(methoxymethyl)-5-phenylfuran 
• 1443441-77-7 2-(naphthalen-1-yl)-5-phenylfuran 
• 119492-84-1 2-phenyl-5-(p-chlorophenyl)furan 
• 94540-81-5 2-(4-methoxyphenyl)-5-phenylfuran 
• 955-83-9 2,5-diphenylfuran 

Relevant articles and documents

A Gold-Catalyzed A3 Coupling/Cyclization/Elimination Sequence as Versatile Tool for the Synthesis of Furfuryl Alcohol Derivatives from Glyceraldehyde and Alkynes

The reaction of glyceraldehyde with alkynes delivers furfuryl alcohol derivatives within only one reaction step in the presence of a gold(III) catalyst. The reaction cascade is initiated by an intermolecular gold-catalyzed A3 coupling sequence in which mo

Synthesis and bioactivity of phenyl substituted furan and oxazole carboxylic acid derivatives as potential PDE4 inhibitors

In this present study, a series of 5-phenyl-2-furan and 4-phenyl-2-oxazole derivatives were designed and synthesized as phosphodiesterase type 4 (PDE4) inhibitors. In vitro results showed that the synthesized compounds exhibited considerable inhibitory ac

PREMATURE-TERMINATION-CODONS READTHROUGH COMPOUNDS

Premature termination codons readthrough compounds, composition thereof, and methods of making and using the same are provided.