B8002
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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
205-982-6
Beilstein/REAXYS Number:
107704
MDL number:
Product Name
2,3-Benzofuran, 99%
InChI key
IANQTJSKSUMEQM-UHFFFAOYSA-N
InChI
1S/C8H6O/c1-2-4-8-7(3-1)5-6-9-8/h1-6H
SMILES string
c1ccc2occc2c1
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
Quality Level
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Related Categories
signalword
Warning
hcodes
Hazard Classifications
Carc. 2 - Flam. Liq. 3
Storage Class
3 - Flammable liquids
wgk
WGK 3
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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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
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.
Javarappa Rangaswamy et al.
Bioorganic & medicinal chemistry letters, 22(14), 4773-4777 (2012-06-15)
In search for a new antioxidant and antimicrobial agent with improved potency, we synthesized a series of benzofuran based 1,3,5-substituted pyrazole analogues (5a-l) in five step reaction. Initially, o-alkyl derivative of salicyaldehyde readily furnish corresponding 2-acetyl benzofuran 2 in good
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)
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
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