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
Regulatory Information
危险化学品
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Satish Kumar et al.
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The Journal of organic chemistry, 76(16), 6488-6502 (2011-06-29)
The central portion of purpuromycin has been assembled via a classical spiroketalization reaction. Key to promoting this reaction mode versus benzofuran formation was the oxidation state of the spiroketal core. With a higher oxidation state, even the electron-deficient isocoumarin found
Romeo Romagnoli et al.
ChemMedChem, 6(10), 1841-1853 (2011-08-02)
Induction of apoptosis is a promising strategy that could lead to the discovery of new molecules active in cancer chemotherapy. This property is generally observed when cells are treated with agents that target microtubules, dynamic structures that play a crucial
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A screening of metals, persistent organic pollutants, pharmaceuticals and personal care products (PPCPs), and other organic contaminants in sludge from seven Swedish sewage treatment plants (STPs) was performed in this study. This extensive screening provides information on mass flows of
Peng Chen et al.
Angewandte Chemie (International ed. in English), 50(35), 8161-8166 (2011-07-13)
Divergent route: a direct C-C bond-forming approach to the key aryl-substituted all-carbon quaternary stereogenic center present in bioactive hydrodibenzofuran alkaloids has been discovered. This approach involves an unprecedented organocatalytic enantioselective Michael addition of α-cyanoketones with acrylates and was used in
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