16191-32-5

Basic information

• Product Name: 2-FURAN-2-YL-BENZALDEHYDE
• Synonyms: 2-(2-FURYL)BENZALDEHYDE;2-FURAN-2-YL-BENZALDEHYDE;AKOS BAR-0077;CHEMBRDG-BB 4003499;VITAS-BB TBB000325;2-(Fur-2-yl)benzaldehyde;2-(2-furyl)benzaldehyde(SALTDATA: FREE);2-(2-Furanyl)benzaldehyde
• CAS NO: 16191-32-5
• Molecular Formula: C₁₁H₈O₂
• Molecular Weight: 172.18
• Mol File: 16191-32-5.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 301.8 °C at 760 mmHg
• Flash Point: 99.2 °C
• Appearance: /
• Density: 1.154 g/cm³
• Vapor Pressure: 0.00103mmHg at 25°C
• Refractive Index: 1.583
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 2-FURAN-2-YL-BENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-FURAN-2-YL-BENZALDEHYDE(16191-32-5)
• EPA Substance Registry System: 2-FURAN-2-YL-BENZALDEHYDE(16191-32-5)

Safety Data

• Hazard Codes: Xi
• Statements: 36
• Safety Statements: 26
• Hazardous Substances Data: 16191-32-5(Hazardous Substances Data)

Usage

General Description

2-FURAN-2-YL-BENZALDEHYDE, also known as furfural, is an organic compound with a strong, sweet, and somewhat almond-like odor. It is a colorless or yellowish oily liquid that is derived from agricultural byproducts and is used in the production of various chemicals, solvents, and resins. Furfural is primarily used as a precursor to various polymers and as a solvent in refining lubricating oils and as a flavoring agent. It is also used in the production of biofuels and as an insecticide and fungicide. Furfural is potentially toxic and can cause irritation to the skin, eyes, and respiratory system.

InChI:InChI=1/C11H8O2/c12-8-9-4-1-2-5-10(9)11-6-3-7-13-11/h1-8H

Upstream product

• 118486-94-5 2-(tributylstannyl)furan 
• 6630-33-7 ortho-bromobenzaldehyde 
• 13331-23-2 fur-2-ylboronic acid 
• 584-12-3 2-bromofuran 
• 40138-16-7 2-formylbenzene boronic acid 
• 497-19-8 sodium carbonate 
• 110-00-9 furan 

Downstream Products

• 4439-57-0 methyl furimidate 
• 617-90-3 2-furancarbonitrile 
• 139697-88-4 2-(α-furyl)benzyl alcohol 
• 1033806-10-8 2,2,2-trifluoro-1-(2-furan-3-yl-phenyl)ethanol 
• 1134426-52-0 (Z)-5-(2-(furan-2-yl)benzylidene)imidazolidine-2,4-dione 
• 1361252-47-2 C₁₄H₁₂O₂ 
• 605-55-0 phenanthren-2-ol 

Relevant articles and documents

Gold(I)-catalyzed furan-yne cyclizations involving 1,2-rearrangement: Efficient synthesis of functionalized 1-naphthols and its application to the synthesis of wailupemycin g

Gold-catalyzed cascade cyclization/1,2-rearrangement of 1-(2-furanyl)phenyl propargyl alcohols has been developed, which provides a rapid and efficient access to multisubstituted 1-naphthols bearing an enal or enone moiety with high stereoselectivity. The (Z)- or (E)-stereochemistry can be easily controlled by choosing protected- or non-protected substrates. The utility of the methodology has been illustrated in the first total synthesis of wailupemycin G.

Gold-catalyzed spirocyclization of furan-ynones and unexpected skeleton rearrangement of the resulting spirohydrofurans

A gold-catalyzed cyclization of aniline-tethered furan-ynones has been developed. The reaction proceeds via trapping of the resulting stabilized cationic intermediate with an amide group leading to polycycles featured with a spiro-cyclohexadienonehydrofur

Based on 4 - phenyl -6 - (2, 2, 2 - trifluoro -1 - phenyl ethoxy) pyrimidine compound and its application method

The present invention relates to compounds based on 4-phenyl-6-(2,2,2-trifluoro-1-phenyl ethoxy) pyrimidine and an application method thereof, particularly discloses compounds of formula I and compositions comprising the compounds, and the application method thereof in treatment, prevention and / or management of diseases or disorders.