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14187-32-7 - Dibenzo-18-crown-6, 98+% - A13133 - Alfa Aesar

A13133 Dibenzo-18-crown-6, 98+%

Numéro CAS
14187-32-7
Synonymes

Dimensions Prix ($) Quantité Disponibilité
5g 21,22
25g 69,73
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Dibenzo-18-crown-6, 98+%

MDL
MFCD00005098
EINECS
238-041-3

Propriétés chimiques

Formule
C20H24O6
Poids formulaire
360.41
Point de fusion
160-164°
Point d'ébullition
380-384°/679mm
Solubilité
Sparingly soluble in water.

Applications

Dibenzo-18-crown-6, is used as an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff. It is an important organic intermediate.

Notes

Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Stable under recommended storage conditions. Incompatible to strong oxidizing agents, strong acids.

Références bibliographiques

PD Beattie.; A Delay.; HH Girault. Investigation of the kinetics of assisted potassium ion transfer by dibenzo-18-crown-6 at the micro-ITIES by means of steady-state voltammetry. Journal of Electroanalytical Chemistry . 1995, 380 (1-2), 167-175.

IM Kolthoff.; MK Chantooni. Transfer activity coefficients in various solvents of several univalent cations complexed withdibenzo-18-crown-6. Jr - Analytical Chemistry. 1980, 380 (1-2), 167-175.

Comparison of the rates of displacement of F- in 1-fluoro-2- or 4-nitrobenzene with KOMe and KO-t-Bu in the presence of this crown ether gave a result (t-BuO- >> MeO-) opposite to the pattern observed in its absence: J. Chem. Soc., Perkin 2, 55 (1973).

Promotes the generation of bromochlorocarbene from Chlorodibromomethane, A16938: Syntheis, 783 (1977); Tetrahedron, 33, 363 (1977), and of dibromocarbene from Bromoform, A11904: Org. Synth., 75, 98 (1997).

In combination with Benzyl­triethyl­ammonium chloride, A13268, promotes the oxidative decarboxylation of arylacetic acids with NaIO4 to give high yields of the aryl aldehydes: Indian J. Chem. B, 35B, 151 (1996). Under the same conditions, phenacyl bromides are converted to benzoic acids.

Catalyst for the formation of phenacyl esters from phenacyl bromides and K salts of carboxylic acids in acetonitrile: Synth. Commun., 26, 1747 (1996).

Catalyst for the halogenative cleavage of epoxides with Br2 or I2, giving halohydrins in high yields: J. Org. Chem., 63, 1455 (1998).

See also 18-Crown-6, A11249 and Appendix 2.

Mentions de danger et de prudence du SGH

Mentions de danger (UE): H315-H319-H335

Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation.

Mentions de prudence: P261-P280-P305+P351+P338-P304+P340-P362-P312-P321-P405-P403+P233-P501a

Avoid breathing dust/fume/gas/mist/vapours/spray. Wear protective gloves/protective clothing/eye protection/face protection. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Take off contaminated clothing and wash before reuse. Call a POISON CENTER or doctor/physician if you feel unwell. Specific treatment (see label). Store locked up. Store in a well-ventilated place. Keep container tightly closed. Dispose of contents/container in accordance with local/regional/national/international regulations.

Autres références

Merck
14,2602
Beilstein
1162153
Code tarifaire harmonisé
2932.99
TSCA
Yes
RTECS
HP5386000

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