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Merck
CN

493449

Sigma-Aldrich

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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About This Item

经验公式(希尔记法):
C9H6O2
CAS号:
分子量:
146.14
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

97%

折射率

n20/D 1.633 (lit.)

bp

135 °C/18 mmHg (lit.)

密度

1.206 g/mL at 25 °C (lit.)

SMILES字符串

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

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一般描述

2-Benzofurancarboxaldehyde, also known as benzo[b]-2-furfural, is an α,β-unsaturated aldehyde.

应用

2-Benzofurancarboxaldehyde may be used in the preparation of (E)-3-(benzofuran-2′-ylmethylidene)-1-methyl-2-indolinone and 1-(benzofuran-2-yl)methanol.

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

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Hydrogenations without hydrogen: titania photocatalyzed reductions of maleimides and aldehydes.
Manley DW, et al.
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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)
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

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