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C109401

Sigma-Aldrich

Cyclooctane

≥99%

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About This Item

Fórmula empírica (notación de Hill):
C8H16
Número de CAS:
292-64-8
Peso molecular:
112.21
Beilstein/REAXYS Number:
1900349
EC Number:
206-031-8
MDL number:
MFCD00004162
UNSPSC Code:
12352100
PubChem Substance ID:
24892341
NACRES:
NA.22

vapor pressure

16 mmHg ( 37.7 °C)

Quality Level

200

assay

≥99%

form

liquid

refractive index

n20/D 1.458 (lit.)

bp

151 °C/740 mmHg (lit.)

mp

10-13 °C (lit.)

density

0.834 g/mL at 25 °C (lit.)

SMILES string

C1CCCCCCC1

InChI

1S/C8H16/c1-2-4-6-8-7-5-3-1/h1-8H2

InChI key

WJTCGQSWYFHTAC-UHFFFAOYSA-N

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Categorías relacionadas

Application

Cyclooctane can undergo oxidation with hydrogen peroxide in the presence of triethylpropylammonium-functionalized silica and transition metal mono-substituted polyoxotungstates.
Cyclooctane may undergo oxidation with hydrogen peroxide in the presence of triethylpropylammonium-functionalized silica and transition metal mono-substituted polyoxotungstates.

pictograms

FlameHealth hazard
GHS02,GHS08

signalword

Danger

hcodes

H226,H304

Hazard Classifications

Asp. Tox. 1 - Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

82.4 °F - closed cup

flash_point_c

28 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Butylcyclohexane ≥99%

Sigma-Aldrich

110388

Butylcyclohexane

Silica supported transition metal substituted polyoxotungstates: Novel heterogeneous catalysts in oxidative transformations with hydrogen peroxide.
Estrada AC, et al.
Applied Catalysis A: General, 392(1-2), 28-35 (2011)
Pieter van Delft et al.
Organic letters, 12(23), 5486-5489 (2010-11-06)
The conjugation of a ribonucleic acid 16-mer with the cationic amphiphilic peptide penetratin and an anionic hyaluronan tetrasaccharide by means of Cu-free "click" chemistry is reported. The alkyne-functionalized 16-mer was prepared by automated solid-phase synthesis, using a newly developed strained
Shawn Martin et al.
The Journal of chemical physics, 132(23), 234115-234115 (2010-06-25)
Understanding energy landscapes is a major challenge in chemistry and biology. Although a wide variety of methods have been invented and applied to this problem, very little is understood about the actual mathematical structures underlying such landscapes. Perhaps the most
Heidi E Bostic et al.
Chemical communications (Cambridge, England), 48(10), 1431-1433 (2011-10-04)
Copper-free click chemistry was employed to derivatize membrane bilayers. This approach uses an azido-lipid conjugate presented on liposomes, which can be labeled in bioorthogonal fashion via cyclooctyne-tagged reagents. An immobilization-based approach using streptavidin-coated microplates was exploited to evaluate membrane derivatization.
The effect of a hydroxy protecting group on the PtCl2-catalyzed cyclization of dienynes--a novel, efficient, and selective synthesis of carbocycles.
Emily Mainetti et al.
Angewandte Chemie (International ed. in English), 41(12), 2132-2135 (2002-06-17)
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