158402
二环己烷并-18-冠醚-6
98%
别名:
2,3,11,12-双环己基-1,4,7,10,13,16-六氧环十八烷, 2,5,8,15,18,21-六氧杂三环[20.4.0.09.14]二十六烷, 二环己基并-18-冠醚-6, 全氢-二苯并-18-冠-6
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关于此项目
经验公式（希尔记法）:
C20H36O6
化学文摘社编号:
分子量:
372.50
UNSPSC Code:
12352302
NACRES:
NA.22
PubChem Substance ID:
EC Number:
240-216-4
Beilstein/REAXYS Number:
1130529
MDL number:
Assay:
98%
Form:
solid
InChI key
BBGKDYHZQOSNMU-UHFFFAOYSA-N
InChI
1S/C20H36O6/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/h17-20H,1-16H2
SMILES string
C1CCC2OCCOCCOC3CCCCC3OCCOCCOC2C1
assay
98%
form
solid
Quality Level
reaction suitability
core: crown ether
functional group
ether
Application
阴离子活化剂，并作为络合剂溶解非极性溶剂中的碱金属离子。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Eye Irrit. 2
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 1
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Aldrichimica Acta, 4, 1-1 (1971)
Aldrichimica Acta, 9, 3-3 (1976)
P Arhem et al.
Acta physiologica Scandinavica, 114(4), 593-600 (1982-04-01)
A potassium carrying ionophore dicyclohexano-18-crown-6 was found to affect the specific ionic currents in the node of Ranvier. Its presence caused an inactivation of the potassium permeability mechanism and a decrease of the sodium permeability. The rate of inactivation of
Giorgio Della Sala et al.
Organic & biomolecular chemistry, 11(5), 726-731 (2012-11-03)
The synthesis, complexation properties and catalytic activities under phase-transfer (PT) conditions of differently substituted cyclohexapeptoids are reported. Association constants, for small cationic alkali, and catalytic performances, in a model nucleophilic substitution, are comparable to those of representative crown ethers. Noteworthy
Negar Bahraini et al.
Health physics, 101(2), 128-135 (2011-06-29)
A molecularly imprinted polymer (MIP) comprising dicyclohexano-18-crown-6 (DCH18C6) was synthesized as a Sr-selective sorbent for urine bioassay purposes. MIP particles (326 ± 2 nm diameter) were formed using acetone and acetonitrile (1:3 v/v) as the porogen, methacrylic acid (MAA) as
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