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526673

5-Phenyl-2-furaldehyde

96%

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About This Item

Empirical Formula (Hill Notation):
C11H8O2
CAS Number:
13803-39-9
Molecular Weight:
172.18
MDL number:
MFCD01910161
UNSPSC Code:
12352100
PubChem Substance ID:
24874570
NACRES:
NA.22

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assay

96%

mp

29-33 °C (lit.)

functional group

aldehyde
phenyl

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

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This Item
440639428558544221
5-Phenyl-2-furaldehyde 96%

Sigma-Aldrich

526673

5-Phenyl-2-furaldehyde

4,5-Dimethyl-2-furaldehyde 97%

Sigma-Aldrich

440639

4,5-Dimethyl-2-furaldehyde

5-(4-Nitrophenyl)-2-furoic acid 96%

Sigma-Aldrich

428558

5-(4-Nitrophenyl)-2-furoic acid

2-Fluoro-5-nitrobenzonitrile 97%

Sigma-Aldrich

544221

2-Fluoro-5-nitrobenzonitrile

assay

96%

assay

97%

assay

96%

assay

97%

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

mp

29-33 °C (lit.)

mp

-

mp

255-257 °C (dec.) (lit.)

mp

76-80 °C (lit.)

functional group

aldehyde

functional group

aldehyde

functional group

carboxylic acid, nitro

functional group

fluoro, nitrile, nitro

General description

5-Phenyl-2-furaldehyde can be prepared from phenylfuran, via formylation.[1] It undergoes electrochemical reduction on a dropping Hg electrode to afford anion radicals in DMF.[2]

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCZ8057
MKCT2594
MKBR2706V
MKBJ5657V
MKBB4048

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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)
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
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

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