thiourea

The global annual production of thiourea is around 10,000 tons.

It is a derivative of thiourea and used as a rodenticide.

There is a large body of evidence linking the ability to taste Thiourea and dietary habits.

The main application of thiourea is in textile processing.

The thiourea route works well with primary halides, especially activated ones.

It is an example of a thiourea.

It can be prepared by the reaction of methyl iodide with thiourea.

Propylthiouracil can be prepared from ethyl 3-oxohexanoate and thiourea.

This white solid is a derivative of thiourea.

Upon cooling, the ammonium salt converts back to thiourea.

The pharmaceuticals thiobarbituric acid and sulfathiazole is prepared using thiourea.

A large group of organocatalysts incorporate the urea or the thiourea moiety.

Bifunctional urea and thiourea catalysis are abundant in the literature.

Other hydrogen-bonded networks are derived from hydroquinone, urea, and thiourea.

In the laboratory, it can also be prepared by the action of 1,2-dibromoethane on thiourea followed by hydrolysis.

Thin films have been deposited, produced from a mixture of citratothallium complex and thiourea.

(2-Chlorophenyl)thiourea is a chemical compound used as an herbicide.

Reaction of β-phenethylamine with ammonium isothiocyanate gives the corresponding thiourea.

This intermediate reduces to diol by thiourea.

The structure of thiourea dioxide is related to that for thiourea.

It condenses with thiourea derivatives to give aminothiazoles.

Many derivatives of thiourea derivatives are useful in organocatalysis.

Similarly, aminothiazoles can be synthesized by the reaction of alpha-halo ketones and thiourea.

Thiourea dioxide is used in reductive bleaching in textiles.

Ethylene thiourea is an organic compound.