B8002
2,3-Benzofuran
99%
Sinónimos:
Coumarone
Iniciar sesiónpara Ver la Fijación de precios por contrato y de la organización
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
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
¿Está buscando productos similares? Visita Guía de comparación de productos
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
Elija entre una de las versiones más recientes:
¿Ya tiene este producto?
Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.
Los clientes también vieron
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
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
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
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
Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.
Póngase en contacto con el Servicio técnico