thionyl

Thionyl chloride can be used to make chemical weapons.

In alternative fashion, the conversion may be performed directly using thionyl chloride.

India is one of a handful of countries making thionyl chloride.

Or the reaction of silver difluoride with thionyl fluoride at 200 degrees.

The reaction with thionyl chloride may be catalyzed by dimethylformamide.

Thionyl chloride can facilitate numerous chemical transformations, some of which are shown below.

Thionyl chloride can be used in variations of the Pummerer rearrangement.

Like thionyl chloride, the reagent produces volatile side products in this application.

"The law will be all over the dude who tries to buy thionyl chloride or a tank of hydrogen now.

In the laboratory, thionyl chloride is especially convenient, because the byproducts are gaseous.

In the laboratory, the conversion can be effected with thionyl chloride:

However, primary amides under heating with thionyl chloride will continue on to form nitriles.

Thionyl chloride is more commonly and more safely employed for this application.

These small devices are powered by a single 3.6-volt lithium thionyl chloride battery, which has a lifetime of six months.

It may also be prepared by treating the hexahydrate with thionyl chloride:

The Administration has called for tough export controls to prevent the sale of poison gas ingredients like thionyl chloride to the third world.

We can restart thionyl chloride synthesization later, when the heat subsides."

The final step in the synthesis is shown below, where thionyl chloride is used to close the pyrrolidine ring.

It can be formed by reacting thionyl chloride with silver sulfide:

Mentioned above, the halide compounds can be made anhydrous by heat, vacuum, or treatment with thionyl chloride.

Alternatively the hydrate can be dehydrated using thionyl chloride.

Formation of acid chloride by treatment with thionyl chloride.

The list includes phosphorous trichloride, trimethyl phosphite and thionyl chloride.

One Pentagon official, who asked not to be identified, expressed confidence that the Army would find alternative supplies of thionyl chloride.

Sulfonic acids react with thionyl chloride to produce sulfonyl chlorides.