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C109401

Sigma-Aldrich

Cyclooctane

≥99%

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About This Item

Fórmula empírica (Notação de Hill):
C8H16
Número CAS:
292-64-8
Peso molecular:
112.21
Beilstein:
1900349
Número CE:
206-031-8
Número MDL:
MFCD00004162
Código UNSPSC:
12352100
ID de substância PubChem:
24892341
NACRES:
NA.22

pressão de vapor

16 mmHg ( 37.7 °C)

Nível de qualidade

200

Ensaio

≥99%

forma

liquid

índice de refração

n20/D 1.458 (lit.)

pb

151 °C/740 mmHg (lit.)

pf

10-13 °C (lit.)

densidade

0.834 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

C1CCCCCCC1

InChI

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

chave InChI

WJTCGQSWYFHTAC-UHFFFAOYSA-N

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Categorias relacionadas

Aplicação

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.

Pictogramas

FlameHealth hazard
GHS02,GHS08

Palavra indicadora

Danger

Frases de perigo

H226,H304

Classificações de perigo

Asp. Tox. 1 - Flam. Liq. 3

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

82.4 °F - closed cup

Ponto de fulgor (°C)

28 °C - closed cup

Equipamento de proteção individual

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

Certificados de análise (COA)

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Cyclooctene oxide 99%

Sigma-Aldrich

C110507

Cyclooctene oxide

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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