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Merck
CN

372293

Benzo-18-crown-6

98%

Synonym(s):

18-Benzo-6-crown ether, 2,3,5,6,8,9,11,12,14,15-Decahydro-1,4,7,10,13,16-benzohexaoxacyclooctadecin, 2,3-Benzo-1,4,7,10,13,16-hexaoxacyclooctadeca-2-ene, Benzo18C6, Monobenzo-18-crown-6

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About This Item

Empirical Formula (Hill Notation):
C16H24O6
CAS Number:
Molecular Weight:
312.36
UNSPSC Code:
12352005
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1626123
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Product Name

Benzo-18-crown-6, 98%

InChI

1S/C16H24O6/c1-2-4-16-15(3-1)21-13-11-19-9-7-17-5-6-18-8-10-20-12-14-22-16/h1-4H,5-14H2

SMILES string

C1COCCOCCOc2ccccc2OCCOCCO1

InChI key

DSFHXKRFDFROER-UHFFFAOYSA-N

assay

98%

mp

42-45 °C (lit.)

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Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)


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Elsayed M Zahran et al.
The Analyst, 142(17), 3241-3249 (2017-08-11)
Electrospray ionization mass spectrometry ESI-MS is a powerful technique for the characterization of macromolecules and their noncovalent binding with guest ions. We herein evaluate the feasibility of using ESI-MS as a screening tool for predicting potentiometric selectivities of ionophores. Ion-selective
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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