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化驗
99%
形狀
liquid
折射率
n20/D 1.462 (lit.)
bp
175-177 °C (lit.)
密度
1.118 g/mL at 25 °C (lit.)
SMILES 字串
CC(=O)OCc1ccco1
InChI
1S/C7H8O3/c1-6(8)10-5-7-3-2-4-9-7/h2-4H,5H2,1H3
InChI 密鑰
CKOYRRWBOKMNRG-UHFFFAOYSA-N
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應用
Furfuryl acetate was used in the synthesis of 5-acetoxymethyl-2-vinylfuran and 5-hydroxymethyl-2-vinylfuran via Vilsmeier-Haack and Wittig reactions.
訊號詞
Warning
危險聲明
危險分類
Acute Tox. 4 Oral
儲存類別代碼
10 - Combustible liquids
水污染物質分類（WGK）
WGK 2
閃點（°F）
150.8 °F - closed cup
閃點（°C）
66 °C - closed cup
個人防護裝備
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
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