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Merck
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B8002

Sigma-Aldrich

2,3-Benzofuran

99%

Sinónimos:

Coumarone

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About This Item

Fórmula empírica (notación de Hill):
C8H6O
Número de CAS:
271-89-6
Peso molecular:
118.13
Beilstein/REAXYS Number:
107704
EC Number:
205-982-6
MDL number:
MFCD00005847
UNSPSC Code:
12352100
PubChem Substance ID:
24892036
NACRES:
NA.22

assay

99%

form

liquid

refractive index

n20/D 1.566 (lit.)

bp

173-175 °C (lit.)

density

1.072 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

c1ccc2occc2c1

InChI

1S/C8H6O/c1-2-4-8-7(3-1)5-6-9-8/h1-6H

InChI key

IANQTJSKSUMEQM-UHFFFAOYSA-N

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Categorías relacionadas

pictograms

FlameHealth hazard
GHS02,GHS08

signalword

Warning

hcodes

H226,H351

Hazard Classifications

Carc. 2 - Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Miyuki Yamaguchi et al.
The Journal of organic chemistry, 78(18), 9270-9281 (2013-08-21)
A dihydroxyterphenylphosphine bearing cyclohexyl groups on the phosphorus atom (Cy-DHTP) was found to be a powerful ligand for the palladium-catalyzed one-pot synthesis of substituted benzo[b]furans from 2-chlorophenols and terminal alkynes. This catalyst system was also applicable to the sequential one-pot
Stefano Protti et al.
The Journal of organic chemistry, 77(15), 6473-6479 (2012-07-11)
2-Substituted benzo[b]furans were synthesized by a one-step metal-free photochemical reaction between 2-chlorophenol derivatives and terminal alkynes by tandem formation of an aryl-C and a C-O bond via an aryl cation intermediate. The mild conditions and the application to chlorophenols rather
Timothy Lynagh et al.
The Journal of biological chemistry, 286(51), 43913-43924 (2011-10-29)
Ivermectin is an anthelmintic drug that works by activating glutamate-gated chloride channel receptors (GluClRs) in nematode parasites. GluClRs belong to the Cys-loop receptor family that also includes glycine receptor (GlyR) chloride channels. GluClRs and A288G mutant GlyRs are both activated
Preetpal Singh Sidhu et al.
Journal of medicinal chemistry, 56(12), 5059-5070 (2013-05-31)
We recently designed a group of novel exosite-2-directed sulfated, small, allosteric inhibitors of thrombin. To develop more potent inhibitors, monosulfated benzofuran tri- and tetrameric homologues of the parent designed dimers were synthesized in seven to eight steps and found to
Xiaomin Liu et al.
Chemical communications (Cambridge, England), 47(43), 11957-11959 (2011-10-05)
The concentration quenching threshold of upconversion luminescence was broken through for the first time via a designed strategy: spatial separation of the emitter doping area.
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