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
Beilstein:
107704
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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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Signal Word
Warning
Hazard Statements
Precautionary 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
Regulatory Information
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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
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
Satish Kumar et al.
Bioorganic & medicinal chemistry, 20(14), 4237-4244 (2012-06-29)
Transmembrane protein 16A (TMEM16A) channels are recently discovered membrane proteins that functions as a calcium activated chloride channel (CaCC). CaCCs are major regulators of various physiological processes, such as sensory transduction, epithelial secretion, smooth muscle contraction and oocyte fertilization. Thirty
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
Andrew N Lowell et al.
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
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