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Diciclohexano-18-corona-6, mezcla de isómeros, 97 %, Thermo Scientific Chemicals

Thermo Scientific Chemicals

Diciclohexano-18-corona-6, mezcla de isómeros, 97 %, Thermo Scientific Chemicals

Name: Diciclohexano-18-corona-6, mezcla de isómeros, 97 %, Thermo Scientific Chemicals
SKU: A15344.03
Price: 31.50 EUR

CAS: 16069-36-6 | C20H36O6 | 372.502 g/mol

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1 g

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25 g

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Número de catálogo A15344.03

también denominado A15344-03

Precio (EUR)

31,50

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Cantidad:

1 g

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Precio (EUR)

31,50

Each

Identificadores químicos

CAS16069-36-6

IUPAC Name2,5,8,15,18,21-hexaoxatricyclo[20.4.0.0⁹,¹⁴]hexacosane

Molecular FormulaC20H36O6

InChI KeyBBGKDYHZQOSNMU-UHFFFAOYNA-N

SMILESC1CCC2OCCOCCOC3CCCCC3OCCOCCOC2C1

Especificaciones Specification Sheet

Hoja de especificaciones

Appearance (Color)White to cream

FormCrystals or powder or crystalline powder or fused solid

Assay (GC)≥96.0%

Identification (FTIR)Conforms

Dicyclohexano is used as an anion activator and complexing agent which solubilizes alkali metal ions in non-polar solvents. It is an important raw material and intermediate used in Organic Synthesis, Pharmaceuticals, Agrochemicals and Dyestuffs etc,.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Aplicaciones
El diciclohexano se utiliza como activador de aniones y agente complejante que solubiliza iones metálicos alcalinos en disolventes no polares. Es una importante materia prima y un intermediario que se utiliza en la síntesis orgánica, productos farmacéuticos, productos agroquímicos, colorantes, etc.

Solubilidad
Soluble en tolueno. Ligeramente soluble (13 g/l, 26 °C) en agua.

Notas
Higroscópico. Almacenénese bajo gas inerte seco. Incompatible con ácidos fuertes y agentes oxidantes fuertes.

RUO – Research Use Only

General References:

Vinod K Gupta; Sudeshna Chandr; Rajni Mangla. Dicyclohexano-18-crown-6 as active material in PVC matrix membrane for the fabrication of cadmium selective potentiometric sensor. Electrochimica Acta.2002, 47 1579-1586.
E. P. Horwitza; M. L. Dietza & D. E. Fishera. Extraction of stoontium from nitric acid solutions using dicyclohexano-18-crown-5 and its derivatives. Electrochimica Acta.1990, 8 557-572.
Crown ether (see Appendix 2). Increases the rate of acetolysis of benzyl chloride in acetonitrile by a factor of >400: Synthesis, 117 (1981).
In combination with potassium permanganate, effects the stereoselective cis-hydroxylation of a double bond from the less-hindered side: Chem. Lett., 173 (1983).