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Merck

138924

Sigma-Aldrich

Cyclooctatetraene

98%

Sinónimos:

[8]Annulene

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About This Item

Fórmula empírica (notación de Hill):
C8H8
Número de CAS:
Peso molecular:
104.15
Beilstein/REAXYS Number:
2496800
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.23

assay

98%

form

liquid

contains

0.1% hydroquinone as inhibitor

refractive index

n20/D 1.537 (lit.)

bp

142-143 °C (lit.)

mp

−5-−3 °C (lit.)

density

0.925 g/mL at 25 °C (lit.)

storage temp.

−20°C

SMILES string

C1=CC=CC=CC=C1

InChI

1S/C8H8/c1-2-4-6-8-7-5-3-1/h1-8H/b2-1-,3-1-,4-2-,5-3-,6-4-,7-5-,8-6-,8-7-

InChI key

KDUIUFJBNGTBMD-BONZMOEMSA-N

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General description

Cyclooctatetraene (COT) is a nonaromatic 4n π-conjugated system with a non-planar tub-shaped geometry and potential energy surfaces at the ground state.
Cyclooctatetraene is an 8p electron system and has a triplet ground state if the p electrons are delocalized. It is antiaromatic hence highly unstable and reactive. It adopts a non-planar boat conformation to attain stability with alternating single and double bonds and hence behaves like a polyolefin.

Application

  • Used in the synthesis of highly organic film for silicon surfaces to improve its chemical and physical properties.
  • Used in liquid state organic dye lasers.
  • Used as triplet state quencher to reduce dye blinking.
COT may be functionalized by two side groups which can be used as active anode materials for rechargeable batteries. High capacity and voltage organic cathodes may be developed by using COT that can be fused with carbon molecules.

signalword

Danger

Hazard Classifications

Aquatic Chronic 3 - Asp. Tox. 1 - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

71.6 °F - closed cup

flash_point_c

22 °C - closed cup

ppe

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


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Aromaticity and antiaromaticity in the low-lying electronic states of cyclooctatetraene.
Karadakov PB.
The Journal of Physical Chemistry A, 112(49), 12707-12713 (2008)
Lauryn E Sass et al.
Biochemistry, 49(14), 3174-3190 (2010-02-26)
The first step in DNA mismatch repair (MMR) is the recognition of DNA mismatches or nucleotide insertions/deletions (IDLs) by MutS and MutS homologues. To investigate the conformational properties of MutS-mismatch complexes, we used single-molecule fluorescence resonance energy transfer (smFRET) to
Erika A Riederer et al.
eLife, 7 (2018-06-12)
Membrane proteins such as ion channels and transporters are frequently homomeric. The homomeric nature raises important questions regarding coupling between subunits and complicates the application of techniques such as FRET or DEER spectroscopy. These challenges can be overcome if the
Structure and bonding of ordered organic monolayers of 1, 3, 5, 7-cyclooctatetraene on the Si (001) surface: Surface cycloaddition chemistry of an antiaromatic molecule
Hovis, Jennifer S., and Robert J. Hamers
The Journal of Physical Chemistry B, 102(4), 687-692 (1998)
Tyson E Graber et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 37(38), 9116-9131 (2017-08-20)
Neuronal mRNAs can be packaged in reversibly stalled polysome granules before their transport to distant synaptic locales. Stimulation of synaptic metabotropic glutamate receptors (mGluRs) reactivates translation of these particular mRNAs to produce plasticity-related protein; a phenomenon exhibited during mGluR-mediated LTD.

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