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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]
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]
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.
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.
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Deuterated dichloromethane (CD 2 Cl 2 or C 2 H 2 Cl 2) [a] is a form (isotopologue) of dichloromethane (DCM, CH 2 Cl 2) in which the hydrogen atoms (H) are deuterium (heavy hydrogen) (2 H or D). [2] Deuterated DCM is not a common solvent used in NMR spectroscopy as it is expensive compared to deuterated chloroform .
Oxalyl chloride reacts with water giving off gaseous products only: hydrogen chloride (HCl), carbon dioxide (CO 2), and carbon monoxide (CO). (COCl) 2 + H 2 O → 2 HCl + CO 2 + CO In this, it is quite different from other acyl chlorides which hydrolyze with formation of hydrogen chloride and the original carboxylic acid.