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质量水平
方案
99%
表单
liquid
折射率
n20/D 1.566 (lit.)
沸点
173-175 °C (lit.)
密度
1.072 g/mL at 25 °C (lit.)
储存温度
2-8°C
SMILES字符串
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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警示用语：
Warning
危险声明
危险分类
Carc. 2 - Flam. Liq. 3
储存分类代码
3 - Flammable liquids
WGK
WGK 3
个人防护装备
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
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
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
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
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