282790
苯并-15-冠醚-5
98%
别名:
2,3,5,6,8,9,11,12-Octahydro-1,4,7,10,13-benzopentaoxacyclopentadecin, 2,3-Benzo-1,4,7,10,13-pentaoxacyclopentadecane, Benzo15C5, Monobenzo-15-crown-5
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关于此项目
经验公式（希尔记法）:
C14H20O5
化学文摘社编号:
分子量:
268.31
UNSPSC Code:
12352005
NACRES:
NA.22
PubChem Substance ID:
EC Number:
237-947-6
Beilstein/REAXYS Number:
1624106
MDL number:
Application
苯并-15-冠醚-5可作为反应剂合成酚类苯并-15-冠醚-5树脂。树脂可进一步通过选择性吸附Li-6同位素，进行锂同位素分离。
General description
苯并-15-冠醚-5是一种大环冠醚。在金属催化反应中可作为配体与金属阳离子配位，增强反应性和选择性。例如，对于某些金属催化的交叉偶联反应，包括Suzuki-Miyaura或Stille反应，它的加入提高了反应的效率和选择性。苯并-15-冠醚-5也可用作有机合成的相转移催化剂。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
J Patrick Shupp et al.
Dalton transactions (Cambridge, England : 2003), 46(28), 9163-9171 (2017-07-05)
We report the synthesis, interconversions and X-ray structures of a set of [mFe-nS]-type carbonyl clusters (where S = S
Li-Jing Du et al.
Food chemistry, 262, 118-128 (2018-05-13)
In this study, dispersive micro solid phase extraction (DMSPE) combined with ultrahigh-performance liquid chromatography coupled with quadrupole time-of-flight tandem mass spectrometry method was established to extract and determine sudan dyes and their metabolites in real samples. The crown ether microfunctionalized
Shinzo Kagabu et al.
Bioorganic & medicinal chemistry letters, 19(11), 2947-2948 (2009-05-05)
Imidacloprid (IMI) derivatives conjugated with benzo-15-crown-5 and benzo-18-crown-6 structures, applied for the first time to explore novel insecticidal molecule, elicited strong excitatory toxic signs to the house flies and stunningly exhibited three to five times higher insecticidal activity than that
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