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Sigma-Aldrich

Furfuryl acetate

99%

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About This Item

Empirical Formula (Hill Notation):
C7H8O3
CAS Number:
623-17-6
Molecular Weight:
140.14
EC Number:
210-775-9
MDL number:
MFCD00003251
UNSPSC Code:
12352100
PubChem Substance ID:
24850158
NACRES:
NA.22

assay

99%

form

liquid

refractive index

n20/D 1.462 (lit.)

bp

175-177 °C (lit.)

density

1.118 g/mL at 25 °C (lit.)

SMILES string

CC(=O)OCc1ccco1

InChI

1S/C7H8O3/c1-6(8)10-5-7-3-2-4-9-7/h2-4H,5H2,1H3

InChI key

CKOYRRWBOKMNRG-UHFFFAOYSA-N

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Application

Furfuryl acetate was used in the synthesis of 5-acetoxymethyl-2-vinylfuran and 5-hydroxymethyl-2-vinylfuran via Vilsmeier-Haack and Wittig reactions.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

10 - Combustible liquids

wgk_germany

WGK 2

flash_point_f

150.8 °F - closed cup

flash_point_c

66 °C - closed cup

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

Certificates of Analysis (COA)

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Alexander Mehner et al.
Molecules (Basel, Switzerland), 12(3), 634-640 (2007-09-14)
5-Acetoxymethyl- and 5-hydroxymethyl-2-vinylfuran were synthesized by two routes. The first route starts from 2-methylfuran and the second from furfuryl acetate. The latter route, involving successive Vilsmeier-Haack and Wittig reactions, is suitable for producing 5-acetoxymethyl-2-vinylfuran and 5-hydroxymethyl-2 vinylfuran in 68% and
R Daniel Cacciari et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 16(11), 1717-1726 (2017-10-27)
The use of biologically active substances with anti-inflammatory properties such as corticosteroids has increased considerably in the last few decades. Particularly, the compound we are interested in, prednisolone (Predn), is a glucocorticoid with high biological activity. This compound absorbs UV

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