Oxalyl chloride is an organic chemical compound with the formula Cl−C(=O)−C(=O)−Cl. This colorless, sharp-smelling liquid, the diacyl chloride of oxalic...

the liberated chloride, forming the acid anhydride and releasing regenerated molecule of DMF. Relative to thionyl chloride, oxalyl chloride is more expensive...

(m.p. 52.5 to 53.5 °C, 126.5 to 128.3 °F). It forms an acid chloride called oxalyl chloride. Transition metal oxalate complexes are numerous, e.g. the...

alcohol (−OH) is oxidized to an aldehyde (−CH=O) or ketone (>C=O) using oxalyl chloride, dimethyl sulfoxide (DMSO) and an organic base, such as triethylamine...

thionyl chloride could be used to make acid anhydrides and acyl chlorides from carboxylic acids and to make alkyl chlorides from alcohols. Oxalyl chloride Phosphorus...

the Ohio River. Carbonyl bromide Carbonyl fluoride Oxalyl chloride Thiophosgene Thionyl chloride Perfluoroisobutene Bis(trifluoromethyl) disulfide Merck...

chlorides, it can be generated from the parent acid and standard chlorinating agents such as phosphorus pentachloride, thionyl chloride, and oxalyl chloride...

that a high-energy intermediate in one of these reactions (between oxalyl chloride and hydrogen peroxide in ethyl acetate), which is presumed to be 1...

chlorinating agents including oxalyl chloride and thionyl chloride. This compound undergoes the reactions common for acid chlorides. For example, it reacts...

vinylene carbonate, which is used in polymers and in organic synthesis. Oxalyl chloride is produced commercially from ethylene carbonate. Photochlorination...