493449
2-苯并呋喃醛
97%
别名:
1-Benzofuran-2-carbaldehyde, 2-Benzofurancarbaldehyde, 2-Formylbenzofuran, Benzo[b]-2-furfural, Benzo[b]furan-2-aldehyde, Benzo[b]furan-2-carboxaldehyde, Coumarilaldehyde
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关于此项目
经验公式（希尔记法）:
C9H6O2
化学文摘社编号:
分子量:
146.14
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
224-248-6
MDL number:
Assay:
97%
Quality Level
assay
97%
refractive index
n20/D 1.633 (lit.)
bp
135 °C/18 mmHg (lit.)
density
1.206 g/mL at 25 °C (lit.)
functional group
aldehyde
SMILES string
O=Cc1cc2ccccc2o1
InChI
1S/C9H6O2/c10-6-8-5-7-3-1-2-4-9(7)11-8/h1-6H
InChI key
ADDZHRRCUWNSCS-UHFFFAOYSA-N
General description
2-Benzofurancarboxaldehyde, also known as benzo[b]-2-furfural, is an α,β-unsaturated aldehyde.
Application
2-Benzofurancarboxaldehyde may be used in the preparation of (E)-3-(benzofuran-2′-ylmethylidene)-1-methyl-2-indolinone and 1-(benzofuran-2-yl)methanol.
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
Telescoped Enolate Arylation/HWE Procedure for the Preparation of 3-Alkenyl-Oxindoles: The First Synthesis of Soulieotine.
Millemaggi A, et al.
European Journal of Organic Chemistry, 2009(18), 2947-2952 (2009)
Hydrogenations without hydrogen: titania photocatalyzed reductions of maleimides and aldehydes.
Manley DW, et al.
Molecules (Basel), 19(9), 15324-15338 (2014)
Niina Tani et al.
Bioorganic & medicinal chemistry, 22(23), 6655-6664 (2014-12-03)
Inhibition of CYP2A6-mediated nicotine metabolism can reduce cigarette smoking. We sought potent and selective CYP2A6 inhibitors to be used as leads for drugs useful in smoking reduction therapy, by evaluating CYP2A6 inhibitory effect of novel formyl, alkyl amine or carbonitrile
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 493449-5G | 04061832406756 |
| 493449-1G | 04061832406749 |