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372293

Benzo-18-crown-6

Name: Benzo-18-crown-6
Brand: ALDRICH

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:

14098-24-9

Molecular Weight:

312.36

UNSPSC Code:

12352005

NACRES:

NA.22

PubChem Substance ID:

24863025

MDL number:

MFCD00062741

Beilstein/REAXYS Number:

1626123

Assay:

98%

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Properties

assay

98%

mp

42-45 °C (lit.)

SMILES string

C1COCCOCCOc2ccccc2OCCOCCO1

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

InChI key

DSFHXKRFDFROER-UHFFFAOYSA-N

Description

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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Correlating the potentiometric selectivity of cyclosporin-based electrodes with binding patterns obtained from electrospray ionization-mass spectrometry.

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

Crown-capped imidacloprid: a novel design and insecticidal activity.

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

Global Trade Item Number

SKU	GTIN
372293-5G	04061831834086