C109401
Cyclooctane
≥99%
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Fórmula empírica (notación de Hill):
C8H16
Número CAS:
Peso molecular:
112.21
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
206-031-8
Beilstein/REAXYS Number:
1900349
MDL number:
Assay:
≥99%
Form:
liquid
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Permítanos ayudarleInChI
1S/C8H16/c1-2-4-6-8-7-5-3-1/h1-8H2
InChI key
WJTCGQSWYFHTAC-UHFFFAOYSA-N
SMILES string
C1CCCCCCC1
vapor pressure
16 mmHg ( 37.7 °C)
assay
≥99%
form
liquid
Quality Level
bp
151 °C/740 mmHg (lit.)
mp
10-13 °C (lit.)
density
0.834 g/mL at 25 °C (lit.)
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.
signalword
Danger
hcodes
Hazard Classifications
Asp. Tox. 1 - Flam. Liq. 3
Clase de almacenamiento
3 - Flammable liquids
wgk
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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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)
Zhong-Ke Yao et al.
Organic letters, 13(1), 134-137 (2010-11-26)
Discovering new carbon building blocks is very significant to advance transition-metal-catalyzed cycloadditions for the synthesis of various-sized ring compounds. A new seven-carbon building block from buta-1,3-dienylcyclopropanes (BDCPs) has been developed, showing that, under the catalysis of [Rh(CO)(2)Cl](2), BDCPs react with
Raffaella Rossin et al.
Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 54(11), 1989-1995 (2013-10-05)
Current pretargeting systems use noncovalent biologic interactions, which are prone to immunogenicity. We previously developed a novel approach based on the bioorthogonal reaction between a radiolabeled tetrazine and an antibody-conjugated trans-cyclooctene (TCO). However, the tumor-to-blood ratio was low due to
Péter Kele et al.
Organic & biomolecular chemistry, 7(17), 3486-3490 (2009-08-14)
The synthesis of a set of new clickable fluorophores that virtually cover the whole visible spectrum reaching the near infra-red regime is presented herein. Besides dyes that are capable of participating in classical copper catalyzed 1,3-dipolar cycloaddition reactions with the
Leo A Paquette et al.
The Journal of organic chemistry, 70(2), 505-509 (2005-01-18)
A program directed to the possible adaptation of ring closing metathesis to a total synthesis of vinigrol is described. With a convenient route to intermediates of general type 3 available from a prior investigation, several candidate substrates were prepared. These
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