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Key Documents

B8002

Sigma-Aldrich

2,3-Benzofuran

99%

Synonym(s):

Coumarone

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About This Item

Empirical Formula (Hill Notation):
C8H6O
CAS Number:
Molecular Weight:
118.13
Beilstein:
107704
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
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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Pictograms

FlameHealth hazard

Signal Word

Warning

Hazard Statements

Hazard Classifications

Carc. 2 - Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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.
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
Highly diastereoselective multicomponent cascade reactions: efficient synthesis of functionalized 1-indanols.
Jun Jiang et al.
Angewandte Chemie (International ed. in English), 52(5), 1539-1542 (2013-01-03)

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