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・ Dichlorine hexoxide
・ Dichlorine monoxide
・ Dichlorine trioxide
・ Dichloro(1,3-bis(diphenylphosphino)propane)nickel
・ Dichloro(cycloocta-1,5-diene)platinum(II)
・ Dichloroacetamide
・ Dichloroacetic acid
・ Dichloroacetylene
・ Dichloroaniline
・ Dichloroarcyriaflavin A synthase
・ Dichlorobenzene
・ Dichlorobis(ethylenediamine)nickel(II)
・ Dichlorobutane
・ Dichlorocarbene
・ Dichlorochromopyrrolate synthase
Dichlorodifluoroethylene
・ Dichlorodifluoromethane
・ Dichlorodifluoromethane (data page)
・ Dichlorodiphenyldichloroethane
・ Dichlorodiphenyldichloroethylene
・ Dichloroethane
・ Dichloroethene
・ Dichlorofluorescein
・ Dichlorofluoromethane
・ Dichloroisocyanuric acid
・ Dichloroisoprenaline
・ Dichloromethane
・ Dichloromethane (data page)
・ Dichloromethane dehalogenase
・ Dichloromethyl methyl ether


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Dichlorodifluoroethylene : ウィキペディア英語版
Dichlorodifluoroethylene

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A dichlorodifluoroethylene (systematically named dichlorodifluoroethene) is one of three compounds with the chemical formula . Dichlorodifluoroethylenes are colourless gases, and are some of the simplest chlorodifluoroalkenes.
The structural isomers are used as intermediates or precursors in the production of other industrial chemicals.〔http://www.buyersguidechem.com/chemical_supplier/1,1-Dichlorodifluoroethylene.php retrieved 26 December 2013〕〔http://www.google.nl/patents/US5118888 retrieved 26 December 2013〕
== 1,1-Dichloro-2,2-difluoroethylene ==

1,1-Dichloro-2,2-difluoroethylene is a low-boiling liquid that is used a refrigerant.〔http://refrigtech.com/Knowledge_Center/Toxic_Info/zsafety.html〕 It may also be used as a solvent, but has practical limitations as such, because of its low boiling point (commercial listings, 19 °C; lit. 17 °C).〔http://www.orgsyn.org/demo.aspx?prep=cv4p0268〕
It is regarded as a hazardous chemical for being toxic by inhalation (see MSDS), and a low-boiling liquid, and it causes irritation when it comes into contact with the skin and mucous membranes. Its ASHRAE number is R-1112a, and its CAS number is 79-35-6. Concentrated 1,1-dichloro-2,2-difluoroethylene can be ignited with ease in the laboratory.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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