It is also a common impurity in sulfur dichloride.

A lot of chlorine would make sulfur dichloride.

It is made by reacting sodium fluoride, chlorine, and sulfur dichloride.

It reacts with chlorine to make sulfur dichloride.

It is obtained by treating sulfur dichloride with chlorine at 193 K:

Sulfur dichloride is the chemical compound with the formula SCl.

Sulfur dichloride is a red liquid.

In 1860, he described combining ethylene with sulfur dichloride and observations of some of the physiological effects it had on him.

It is isoelectronic to sulfur dichloride.

It is an unstable pale yellow solid, decomposing to sulfur dichloride and chlorine at temperatures above 242 K.

Sulfur dichloride and disulfur dichloride are important industrial chemicals.

Sulfur dichloride, also known as sulfur(II) chloride, is a chemical compound.

The major industrial synthesis involves the reaction of sulfur trioxide and sulfur dichloride:

It is possible to remove the more volatile byproducts such as carbon tetrachloride and sulfur dichloride from the reaction mixture by distillation.

Dibenzothiophene is prepared by the reaction of biphenyl with sulfur dichloride in the presence of aluminium trichloride.

Other methods include syntheses from phosphorus pentachloride, chlorine and sulfur dichloride, or phosgene:

In particular, selenium dichloride and sulfur dichloride can react to form organic selenium compounds.

Sulfur trioxide also reacts with sulfur dichloride to yield the useful reagent, thionyl chloride.

In the Depretz method, sulfur mustard is synthesized by treating sulfur dichloride with ethylene:

The reaction of polysulfanes with sulfur dichloride or disulfur dichloride produces long-chain dichloropolysulfanes:

It can be generated by the reaction of sulfur dichloride and potassium fluoride or mercury(II) fluoride at low pressures:

In analogy to sulfur dichloride, it hydrolyzes in water to give hydrogen bromide, sulfur dioxide and elemental sulfur.

The primary unwanted byproducts of this reaction are sulfur dichloride, sulfur chloride (sulfur monochloride) and carbon tetrachloride.

Despretz described the reaction of sulfur dichloride and ethylene but never made mention of any irritating properties of the reaction product, which makes the claim doubtful.

A yellow oil, it is prepared by reaction of tert-butylamine with sulfur dichloride to give the intermediate "S(N-t-Bu)", which decomposes at 60 C to give the diimide.