Quality Level
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.)
functional group
ester
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
Application
Furfuryl acetate was used in the synthesis of 5-acetoxymethyl-2-vinylfuran and 5-hydroxymethyl-2-vinylfuran via Vilsmeier-Haack and Wittig reactions.
Still not finding the right product?
Explore all of our products under 醋酸糠酯
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
10 - Combustible liquids
wgk
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)
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
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 166200-25G | 04061838748843 |