D62403
1,2-Dichloroethylene, mixture of cis and trans
98%
Synonyme(s) :
1,2-Dichloroethene, Acetylene dichloride, sym-Dichloroethylene
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About This Item
Formule linéaire :
ClCH=CHCl
Numéro CAS:
Poids moléculaire :
96.94
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22
Produits recommandés
Pression de vapeur
5.32 psi ( 20 °C)
Pureté
98%
Forme
liquid
Indice de réfraction
n20/D 1.447 (lit.)
Point d'ébullition
48-60 °C (lit.)
Pf
−57 °C (lit.)
Densité
1.265 g/mL at 25 °C (lit.)
Chaîne SMILES
Cl\C=C\Cl
InChI
1S/C2H2Cl2/c3-1-2-4/h1-2H/b2-1+
Clé InChI
KFUSEUYYWQURPO-OWOJBTEDSA-N
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Description générale
1,2-Dichloroethylene, also known as acetylene dichloride, is a chlorinated aliphatic hydrocarbon that is commonly used as an extraction solvent and as a chemical intermediate for other chlorinated solvents and compounds.
Application
1,2-Dichloroethylene, mixture of cis and trans can be used as a reactant to synthesize:
- Chloro-enynes from terminal alkynes via Sonogashira coupling.
- Trichloroethyl alkyl ketones by reacting with acyl chlorides via Friedel-Crafts reaction in the presence of aluminum chloride.
- (Ethenediyl)bis[thiazole] via Pd-catalyzed Stille-coupling reaction with 2-(tributylstannyl)thiazole.
À utiliser avec
Réf. du produit
Description
Tarif
Mention d'avertissement
Danger
Mentions de danger
Conseils de prudence
Classification des risques
Acute Tox. 4 Inhalation - Aquatic Chronic 3 - Flam. Liq. 2
Code de la classe de stockage
3 - Flammable liquids
Classe de danger pour l'eau (WGK)
WGK 2
Point d'éclair (°F)
42.8 °F - closed cup
Point d'éclair (°C)
6 °C - closed cup
Équipement de protection individuelle
Eyeshields, Faceshields, Gloves
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Les clients ont également consulté
Jisu Hong et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 25(2), 649-656 (2018-11-06)
The effects of the molecular structure of thiazole-based polymers on the active layer morphologies and performances of electronic and photovoltaic devices were studied. Thus, thiazole-based conjugated polymers with a novel thiazole-vinylene-thiazole (TzVTz) structure were designed and synthesized. The TzVTz structure
C Andrew Ramsburg et al.
Environmental science & technology, 44(23), 9105-9111 (2010-11-09)
Abiotic and biotic reductive dechlorination with chlorinated ethene dense non-aqueous-phase liquid (DNAPL) source zones can lead to significant fluxes of complete and incomplete transformation products. Accurate assessment of in situ rates of transformation and the potential for product sequestration requires
Florian Schevenels et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 19(13), 4335-4343 (2013-01-22)
Highly functionalised benzofurans have been prepared from ortho-hydroxyphenones and 1,1-dichloroethylene. The key intermediate, a chloromethylene furan, smoothly rearranged into the corresponding benzofuran carbaldehyde under acidic conditions. Some mechanistic investigations have been performed and several biologically active benzofurans have been synthesised.
He-Ping Zhao et al.
Water research, 44(7), 2276-2282 (2010-01-19)
The presence of other chloroethenes influences aerobic metabolic biodegradation of cis-1,2-dichloroethene (cDCE). A new metabolically cDCE degrading enrichment culture was identified as also being capable of degrading vinyl chloride (VC), but not 1,1-dichloroethene (1,1DCE), trans-1,2-dichloroethene (tDCE), trichloroethene (TCE), or tetrachloroethene
He-Ping Zhao et al.
Water science and technology : a journal of the International Association on Water Pollution Research, 64(9), 1796-1803 (2011-10-25)
Degradation of the lower chlorinated ethenes is crucial to the application of natural attenuation or in situ bioremediation on chlorinated ethene contaminated sites. Recently, within mixtures of several chloroethenes as they can occur in contaminated groundwater inhibiting effects on aerobic
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