196398
呋喃-3-甲醇
99%
别名:
3-呋喃甲醇
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关于此项目
经验公式（希尔记法）:
C5H6O2
化学文摘社编号:
分子量:
98.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
224-570-7
Beilstein/REAXYS Number:
106456
MDL number:
产品名称
呋喃-3-甲醇, 99%
InChI key
STJIISDMSMJQQK-UHFFFAOYSA-N
InChI
1S/C5H6O2/c6-3-5-1-2-7-4-5/h1-2,4,6H,3H2
SMILES string
OCc1ccoc1
assay
99%
form
liquid
refractive index
n20/D 1.484 (lit.)
bp
79-80 °C/17 mmHg (lit.)
density
1.139 g/mL at 25 °C (lit.)
functional group
hydroxyl
Quality Level
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Application
Furan-3-methanol was used in the synthesis of substituted δ2-butenolides and 1-benzyl-3-(furan-3-ylmethyl)-3-methylpyrrolidin-2-one.
General description
Furan-3-methanol on oxidation with pyridinium chlorochromate yields furan-3-carboxaldehyde.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
100.4 °F - closed cup
flash_point_c
38 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
3-Alkylfurans as useful synthetic equivalents for substituted δ2-butenolides.
Goldsmith D, et al.
Tetrahedron Letters, 24(52), 5835-5838 (1983)
Stannylation/destannylation. Preparation of. alpha.-alkoxy organolithium reagents and synthesis of dendrolasin via a carbinyl carbanion equivalent.
Still WC.
Journal of the American Chemical Society, 100(5), 1481-1487 (1978)
Jai K Chavda et al.
European journal of organic chemistry, 2014(1), 129-139 (2014-05-16)
The tricyclic BCD substructure of the marine natural product nakadomarin A has been synthesised. The strategy utilised a key carbon-carbon bond-forming reaction between a furan and an
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