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526673

Sigma-Aldrich

5-Phenyl-2-furaldehyde

96%

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About This Item

Empirical Formula (Hill Notation):
C11H8O2
CAS Number:
Molecular Weight:
172.18
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

96%

mp

29-33 °C (lit.)

SMILES string

O=Cc1ccc(o1)-c2ccccc2

InChI

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

InChI key

BMJHNNPEPBZULA-UHFFFAOYSA-N

General description

5-Phenyl-2-furaldehyde can be prepared from phenylfuran, via formylation. It undergoes electrochemical reduction on a dropping Hg electrode to afford anion radicals in DMF.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Cathodic reduction of substituted 5-phenyl-2-furaldehydes in dimethylformamide.
Cernak J, et al.
Chemical Papers, 34(6), 788-792 (1980)
Furan derivatives. XXXI.< x,/MJnsaturated ketones of the phenylfuran series.
Frimm R, et al.
Chem. Zeit., 27(1), 101-106 (1973)
Kyungsil Yoon et al.
Cells, 8(3) (2019-03-15)
Chicken ovalbumin upstream promoter-transcription factor I (COUP-TFI) is an orphan receptor and member of the nuclear receptor superfamily. Among a series of methylene substituted diindolylmethanes (C-DIMs) containing substituted phenyl and heteroaromatic groups, we identified 1,1-bis(3'-indolyl)-1-(4-pyridyl)-methane (DIM-C-Pyr-4) as an activator of
Renzo P Zanocco et al.
PloS one, 13(7), e0200006-e0200006 (2018-07-03)
In this study, we report the synthesis and the photochemical behavior of a series of new "click-on" fluorescent probes designed to detect singlet oxygen. They include a highly fluorescent chemical structure, an aryloxazole ring, linked to a furan moiety operating

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