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Wichtige Dokumente
278343
1,2,4,5-Tetrabrombenzol
97%
Synonym(e):
2,3,5,6-Tetrabromobenzene
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Alle Fotos(2)
About This Item
Empirische Formel (Hill-System):
C6H2Br4
CAS-Nummer:
Molekulargewicht:
393.70
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
Empfohlene Produkte
Assay
97%
mp (Schmelzpunkt)
180-182 °C (lit.)
Funktionelle Gruppe
bromo
SMILES String
Brc1cc(Br)c(Br)cc1Br
InChI
1S/C6H2Br4/c7-3-1-4(8)6(10)2-5(3)9/h1-2H
InChIKey
QCKHVNQHBOGZER-UHFFFAOYSA-N
Allgemeine Beschreibung
The single structure of 1,2,4,5-tetrabromobenzene as actuating elements was studied and the relations between their mechanical properties and kinematic profile were determined.
Anwendung
1,2,4,5-Tetrabromobenzene has been used in the synthesis of diethynyltriptycene-linked dipyridyl ligands.
Signalwort
Warning
H-Sätze
Gefahreneinstufungen
Aquatic Chronic 4 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Zielorgane
Respiratory system
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
dust mask type N95 (US), Eyeshields, Gloves
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Organic letters, 7(21), 4585-4588 (2005-10-08)
[reaction: see text] An efficient route to a new family of dinucleating ligands has been developed. A convergent strategy to these ligands involved dual Sonogashira cross-coupling of 2,3-diethynyltriptycene with a variety of functionally diverse 5-bromopyridines. The resultant ligands were accessed
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Journal of the American Chemical Society, 135(37), 13843-13850 (2013-07-31)
A paradigm shift from hard to flexible, organic-based optoelectronics requires fast and reversible mechanical response from actuating materials that are used for conversion of heat or light into mechanical motion. As the limits in the response times of polymer-based actuating
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