232017

Chloranil

99%

• Synonym(e): 2,3,5,6-Tetrachlor-1,4-benzochinon, p-Chloranil, Tetrachlor-1,4-benzochinon
• Lineare Formel: C₆Cl₄(=O)₂
• CAS-Nummer: 118-75-2
• Molekulargewicht: 245.88
• Beilstein: 393006
• EG-Nummer: 204-274-4
• MDL-Nummer: MFCD00001594
• UNSPSC-Code: 12162002
• PubChem Substanz-ID: 24853870
• NACRES: NA.23

Eigenschaften

• Qualitätsniveau: 200
• Assay: 99%
• Form: solid
• mp (Schmelzpunkt): 289 °C (dec.) (lit.)
• SMILES String: ClC1=C(Cl)C(=O)C(Cl)=C(Cl)C1=O
• InChI: 1S/C6Cl4O2/c7-1-2(8)6(12)4(10)3(9)5(1)11
• InChIKey: UGNWTBMOAKPKBL-UHFFFAOYSA-N
• Angaben zum Gen: human ... ACHE(43) , BCHE(590) , CES1(1066)

Beschreibung

Allgemeine Beschreibung

Tetrachloro-1,4-benzoquinone (TCBQ) is a quinone compound with four chloride groups. The catalytic activity of quinone groups (benzoquinone) can be controlled by the chloride groups with large electronegativity.

Anwendung

Synthesis of dibenzofurans via oxidative cyclization.

Undergoes photoinduced cycloaddition reactions with stilbene derivatives and α,β-unsaturated carbonyl compounds. Fluorescence quencher.

TCBQ can form a nanocomposite with multi-walled carbon nanotubes (MWCNTs) on a graphite electrode for nicotinamide adenine dinucleotide (NADH) oxidation. It can also provide pseudocapacitance and can be used as an electrode material for the development of supercapacitors. It may be used as an organic cathode and act as a redox mediator for the fabrication of lithium ion batteries.

Sicherheitshinweise

• Piktogramme: GHS05,GHS07,GHS09
• Signalwort: Danger
• H-Sätze: H315,H317,H318,H410
• P-Sätze: P261 - P264 - P273 - P280 - P302 + P352 - P305 + P351 + P338
• Gefahreneinstufungen: Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1
• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 2
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable
• Persönliche Schutzausrüstung: dust mask type N95 (US), Eyeshields, Gloves