M46845
2-甲基呋喃
contains 200-400 BHT as stabilizer, 99%
别名:
邻甲呋喃
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关于此项目
经验公式（希尔记法）:
C5H6O
化学文摘社编号:
分子量:
82.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-594-5
Beilstein/REAXYS Number:
103733
MDL number:
产品名称
2-甲基呋喃, contains 200-400 BHT as stabilizer, 99%
InChI key
VQKFNUFAXTZWDK-UHFFFAOYSA-N
InChI
1S/C5H6O/c1-5-3-2-4-6-5/h2-4H,1H3
SMILES string
Cc1ccco1
vapor density
2.8 (vs air)
vapor pressure
139 mmHg ( 20 °C)
561 mmHg ( 55 °C)
assay
99%
form
liquid
contains
200-400 BHT as stabilizer
refractive index
n20/D 1.433 (lit.)
bp
63-66 °C (lit.)
density
0.91 g/mL at 25 °C (lit.)
Quality Level
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Application
2-甲基呋喃可用于通过与马来酸酐的 Diels-Alder 反应合成 外-顺 -1-甲基-7-氧杂双环 [2.2.1] 庚烯-2,3-二羧酸酐。
General description
取代呋喃 2-甲基呋喃被认为是内燃机的潜在替代燃料。对其微波谱进行了分析。碳源在不同反应条件下合成 2-MF 已有报道。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 2 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2
存储类别
3 - Flammable liquids
wgk
WGK 1
flash_point_f
-7.6 °F
flash_point_c
-22 °C
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Combustion performance and emissions of 2-methylfuran diesel blends in a diesel engine.
Xiao H, et al.
Fuel: The Science and Technology of Fuel and Energy, 175, 157-163 (2016)
Renewable production of phthalic anhydride from biomass-derived furan and maleic anhydride.
Mahmoud E, et al.
Green Chemistry, 16(1), 167-175 (2014)
V Ravindranath et al.
Toxicology and applied pharmacology, 85(1), 78-91 (1986-08-01)
Administration of a single ip dose of 2-methylfuran (2-MF) to male Sprague-Dawley rats at a dose of 100 mg/kg produced centrilobular necrosis of the liver and bronchial injury of the lung, the severity of the lesions increasing with increasing doses
Guangyi Li et al.
ChemSusChem, 5(10), 1958-1966 (2012-08-22)
Hydroxyalkylation-alkylation (HAA) coupled with hydrodeoxygenation is a promising route for the synthesis of renewable high-quality diesel or jet fuel. In this work, a series of solid-acid catalysts were firstly used for HAA between lignocellulose-derived furan and carbonyl compounds. Among the
V Ravindranath et al.
Science (New York, N.Y.), 224(4651), 884-886 (1984-05-25)
An important mechanism of toxicity of furans involves the cytochrome P-450 monooxygenase-catalyzed bioactivation of the compound in situ directly within the target tissues to highly reactive electrophilic products. The unsaturated aldehydes acetylacrolein and methylbutenedial have been identified as the principal
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