B8002
2,3-Benzofuran
99%
Sinónimos:
Coumarone
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About This Item
Fórmula empírica (notación de Hill):
C8H6O
Número de CAS:
Peso molecular:
118.13
Beilstein/REAXYS Number:
107704
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
form:
liquid
assay:
99%
Productos recomendados
Quality Level
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
signalword
Warning
hcodes
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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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
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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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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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