Oxidation Reagents

Octyl acetate.

Oxalyl bromide.

Oxalyl bromide.

DescriptionUsed in synthetic applications of carbon-substituted iminium saltsReactant for:Synthesis of mutasynthons added to cultures ofA. pretiosumfor mutasynthetic generation of ansamitocin derivativesOxalic acid formation from hydroxyl radical

DescriptionUsed in synthetic applications of carbon-substituted iminium saltsReactant for:Synthesis of mutasynthons added to cultures ofA. pretiosumfor mutasynthetic generation of ansamitocin derivativesOxalic acid formation from hydroxyl radical

General DescriptionOxalyl chloride is a commonly used chlorinating reagent that can be prepared by the reaction of oxalic acid and phosphorus pentachloride.ApplicationOxalyl chloride may be used in the following processes: Preparation of Mosher′s

General DescriptionOxalyl chloride is a commonly used chlorinating reagent that can be prepared by the reaction of oxalic acid and phosphorus pentachloride.ApplicationOxalyl chloride may be used in the following processes: Preparation of Mosher′s

General DescriptionOxalyl chloride is a commonly used chlorinating reagent that can be prepared by the reaction of oxalic acid and phosphorus pentachloride.ApplicationOxalyl chloride may be used in the following processes: Preparation of Mosher′s

General DescriptionOxalyl chloride is a commonly used chlorinating reagent that can be prepared by the reaction of oxalic acid and phosphorus pentachloride.ApplicationOxalyl chloride may be used in the following processes: Preparation of Mosher′s

Application：Oxalyl chloride is generally used as a dimethyl sulfoxide activator and a chlorinating agent to convert carboxylic acid to acid chlorides.

Application：Oxalyl chloride is generally used as a dimethyl sulfoxide activator and a chlorinating agent to convert carboxylic acid to acid chlorides.

Oxalyldihydrazide was used as a crosslinker for enrichment of carbonylated proteins within a microfluid chip. It was also used to synthesize a new series of manganese and iron salt forming complexes by template condensation with glyoxal.