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Key Documents

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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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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

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Certificados de análisis (COA)

Lot/Batch Number
SHBQ7874
SHBP3947
SHBK3666
SHBK1739
SHBK1738

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Sigma-Aldrich

C110507

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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)
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.
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
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)
Gökhan Ceyhan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 95, 382-398 (2012-05-11)
Three Schiff base ligands (H(2)L(1)-H(2)L(3)) with N(2)O(2) donor sites were synthesized by condensation of 1,5-diaminonapthalene with benzaldehyde derivatives. A series of Cu(II), Co(II), Ni(II), Mn(II) and Cr(III) complexes were prepared and characterized by spectroscopic and analytical methods. Thermal, electrochemical and
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