48190
(±)-1-(2-呋喃基)乙醇
≥99.0% (GC)
别名:
(±)-α-甲基呋喃-2-甲醇, (±)-2-呋喃基甲基甲醇
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关于此项目
经验公式（希尔记法）:
C6H8O2
化学文摘社编号:
分子量:
112.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
224-130-4
Beilstein/REAXYS Number:
107814
MDL number:
Assay:
≥99.0% (GC)
Quality Level
assay
≥99.0% (GC)
contains
~0.05% hydroquinone as stabilizer
refractive index
n20/D 1.479
bp
167-170 °C
density
1.078 g/mL at 20 °C (lit.)
functional group
hydroxyl
storage temp.
2-8°C
SMILES string
CC(O)c1ccco1
InChI
1S/C6H8O2/c1-5(7)6-3-2-4-8-6/h2-5,7H,1H3
InChI key
UABXUIWIFUZYQK-UHFFFAOYSA-N
General description
(±)-1-（2-呋喃基）乙醇 [(±)-2-呋喃甲基甲醇] 是呋喃衍生物。报道了由 2-呋喃甲基甲醇合成 4-羟基-2-甲基环戊烯-2-烯-1-酮的方法。
Application
(±)-1-（2-呋喃基）乙醇（外消旋 1-（2-呋喃基）乙醇）可用于 1-乙酰氧基-1-[2-呋喃基]乙烷的合成。
Disclaimer
储存时可能变为棕色
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
Eyeshields, Gloves
法规信息
新产品
此项目有
An Enantioselective Total Synthetic Approach to (+)-Heptemerone G and (+)-Guanacastepene A from 2-Furyl Methyl Carbinol.
Michalak K and Wicha J.
Synlett, 24, 1387-1390 (2013)
A Ghanem et al.
Chirality, 13(2), 118-123 (2001-02-15)
Asymmetric acetylation of racemic 1-(2-furyl)ethanol with the innocuous acyl donor isopropenyl acetate catalyzed by lipases in organic media afforded the chiral alcohol and acetate in high enantiomeric excess (up to 99%). The effect of molecular sieves as well as organic
Jordan Lopez et al.
Journal of agricultural and food chemistry, 67(41), 11444-11453 (2019-10-09)
Innovative approaches to develop flavors with high sensory appeal are critical in encouraging increased consumer preference and adoption of low sodium foods. Gas chromatography-olfactometry, coupled with stable isotope dilution assays and sensory experiments, led to the identification of the odorants
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 48190-10ML-F | 04061832389073 |