Ciclohexilacetileno, 98 %, Thermo Scientific Chemicals

Name: Ciclohexilacetileno, 98 %, Thermo Scientific Chemicals
SKU: H53418.06

CAS: 931-48-6 | C8H12 | 108.184 g/mol

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5 g

25 g

Número de catálogo H53418.06

también denominado H53418-06

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5 g

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Identificadores químicos

CAS931-48-6

IUPAC Nameethynylcyclohexane

Molecular FormulaC8H12

InChI KeySSDZYLQUYMOSAK-UHFFFAOYSA-N

SMILESC#CC1CCCCC1

Especificaciones Specification Sheet

Hoja de especificaciones

FormLiquid

Assay (GC)>97.5%

Appearance (Color)Colorless

Cyclohexylacetylene is used in the preparation of hydrido-vinylidene complexes of osmium, which finds vital intermediates in several homogeneous and heterogeneous catalytic reactions such as alkene olimerization, polymerization and Fischer-Tropsch synthesis.

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 ciclohexilacetileno se utiliza en la preparación de complejos hidrido-vinilideno de osmio, que encuentra intermedios vitales en varias reacciones catalíticas homogéneas y heterogéneas como la olimerización alquena, la polimerización y la síntesis de Fischer-Tropsch.

Solubilidad
No miscible con agua.

Notas
Incompatible con agentes oxidantes fuertes.

RUO – Research Use Only

General References:

Jacquet, J.; Auvinet, A. L.; Mandadapu, A. K.; Haddad, M.; Ratovelomanana-Vidal, V.; Michelet, V. Practical Solvent-Free Ruthenium Trichloride-Mediated Benzannulation Approach to Fused Functionalized Arenes. Adv. Synth. Catal. 2015, 357 (7), 1387-1392.
Zhang, A. L.; Yang, L. W.; Yang, N. F.; Zhang, J. Synthesis of enantiopure C₃-symmetric bulky trialkanolamines and their enantioselective inductivity during the alkynylation of aldehydes. J. Organomet. Chem. 2015, 775, 88-93.