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Dichloromethane (DCM, methylene chloride, or methylene bichloride) is an organochlorine compound with the formula C H 2 Cl 2. This colorless, volatile liquid with a chloroform-like, sweet odor is widely used as a solvent. Although it is not miscible with water, it is slightly polar, and miscible with many organic solvents. [12]
6 Structure and properties data. ... Please find below supplementary chemical data about dichloromethane. ... log 10 of Dichloromethane vapor pressure. Uses formula: ...
1,2-Dichloroethylene or 1,2-DCE is the name for a pair of organochlorine compounds with the molecular formula C 2 H 2 Cl 2. The two compounds are isomers, each being colorless liquids with a sweet odor. It can exist as either of two geometric isomers, cis-1,2-dichloroethene or trans-1,2-dichloroethene, but is often used as a mixture of the two ...
Dichlorocarbene is an intermediate in the carbylamine reaction. In this conversion, a dichloromethane solution of a primary amine is treated with chloroform and aqueous sodium hydroxide in the presence of catalytic amount of the phase-transfer catalyst. Illustrative is the synthesis of tert-butyl isocyanide: [7]
The most important is dichloromethane, which is mainly used as a solvent. Chloromethane is a precursor to chlorosilanes and silicones . Historically significant (as an anaesthetic), but smaller in scale is chloroform, mainly a precursor to chlorodifluoromethane (CHClF 2 ) and tetrafluoroethene which is used in the manufacture of Teflon.
1,1-Dichloroethylene, commonly called vinylidene chloride or 1,1-DCE, is an organochloride with the molecular formula CCl 2 CH 2.It is a colorless liquid with a sharp odor. Like most chlorocarbons, it is poorly soluble in water but soluble in organic solvents. 1,1-DCE was the precursor to the original clingwrap, Saran, for food, but this application has been phased
The reaction uses a hypervalent iodine reagent [2] similar to 2-iodoxybenzoic acid to selectively and mildly oxidize alcohols to aldehydes or ketones. The reaction is commonly conducted in chlorinated solvents such as dichloromethane or chloroform. [2] The reaction can be done at room temperature and is quickly complete.
A typical PCC oxidation involves addition of an alcohol to a suspension of PCC in dichloromethane. [6] [7] [8] The general reaction is: 2 [C 5 H 5 NH][CrO 3 Cl] + 3 R 2 CHOH → 2 [C 5 H 5 NH]Cl + Cr 2 O 3 + 3 R 2 C=O + 3 H 2 O. For example, the triterpene lupeol was oxidized to lupenone: [9]