33531
二苯并-18-冠醚-6
purum, ≥98.0% (UV)
别名:
2,3,11,12-二苯并-1,4,7,10,13,16-六氧杂环十八-2,11-二烯, 6,7,9,10,17,18,20,21-八氢二苯并[b,k][1,4,7,10,13,16]六氧杂环十八碳烯, DB18C6
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关于此项目
经验公式（希尔记法）:
C20H24O6
化学文摘社编号:
分子量:
360.40
EC Number:
238-041-3
UNSPSC Code:
12350000
PubChem Substance ID:
Beilstein/REAXYS Number:
1162153
MDL number:
grade
purum
assay
≥98.0% (UV)
mp
161-163 °C, 162-164 °C (lit.)
SMILES string
C1COc2ccccc2OCCOCCOc3ccccc3OCCO1
InChI
1S/C20H24O6/c1-2-6-18-17(5-1)23-13-9-21-11-15-25-19-7-3-4-8-20(19)26-16-12-22-10-14-24-18/h1-8H,9-16H2
InChI key
YSSSPARMOAYJTE-UHFFFAOYSA-N
Other Notes
阳离子大环络化剂
法规信息
新产品
此项目有
F. Vogtle et al.
Topics in Current Chemistry, 98 (1981)
Ying Han et al.
The Journal of organic chemistry, 77(5), 2422-2430 (2012-02-11)
A new triptycene-derived macrotricyclic host containing two dibenzo-[18]-crown-6 moieties was synthesized and shown to form 1:1 complexes with paraquat derivatives in solution, in which the guests all thread the central cavity of the host. However, it was interestingly found that
A Carabez et al.
Biochimica et biophysica acta, 638(1), 125-131 (1981-11-12)
In rat liver mitochondria, the macrocyclic polyether, dibenzo-18-crown-6 (polyether XXVIII) inhibits the oxidation of NAD-dependent substrates, as stimulated by ADP, uncouplers and valinomycin plus K+. It does not inhibit the oxidation of succinate. It is concluded that polyether XXVIII inhibits
L A Shahada
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 61(8), 1795-1798 (2005-05-03)
The interaction of the crown ether dibenzo-18-crown-6 (DBC) with iodine has been studied in CHCl3 at room temperature. The charge-transfer absorptions, far infrared and thermal measurements of the formed charge-transfer complex were recorded and discussed. The results obtained show the
Yuchuan Cheng et al.
Journal of colloid and interface science, 307(2), 447-454 (2007-01-09)
Reported here is the study on the structure of Langmuir-Blodgett (LB) films of double-armed dibenzo-18-crown-6 contain biphenyl (DACE) which are newly synthesized and mixed with stearic acid (SA). In addition, the miscibility of the two compounds was also tested by
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