54742-57-3

Usage

Structure

A five-membered ring containing three nitrogen atoms and two sulfur atoms, with a carbonyl chloride group attached to the 5th position.

Type of compound

Carbonyl chloride derivative of 1,2,3-thiadiazole

Applications

a. Versatile building block in organic synthesis
b. Preparation of heterocycles and pharmaceuticals
c. Potential applications in the development of new drugs
d. Use in materials science

Reactivity

Reactive compound

Hazardous nature

Potentially hazardous compound

Safety protocols

Should be handled with care and in accordance with proper safety protocols.

Upstream product

• 4833-09-4 1,2,3-thiadiazole-5-carboxylic acid 
• 79-37-8 oxalyl dichloride 

Relevant academic research and scientific papers

Preparation and promotion of fruit growth in kiwifruit of fluorinated N-phenyl-N′-1,2,3-thiadiazol-5-yl ureas

Seventeen phenyl-fluorinated analogues of thidiazuron [N-phenyl-N′- (1,2,3-thiadiazol-5-yl)urea, TDZ] have been prepared and characterized. The effects of each fluorinated urea on growth and quality of kiwifruits (Actinidia deliciosa) were evaluated by co

HERBICIDAL COMPOUNDS

The present invention relates to herbicidally active thiadiazole derivatives, as well as to processes and intermediates used for the preparation of such derivatives. The invention further extends to herbicidal compositions comprising such derivatives, as well as to the use of such compounds and compositions in controlling undesirable plant growth: in particular the use in controlling weeds, in crops of useful plants.

Method of treating a patient having precancerous lesions with quinazoline derivatives

Derivatives of Quinazoline are useful for the treatment of patients having precancerous lesions. These compounds are also useful to inhibit growth of neoplastic cells.

1,2,3-THIADIAZOLE AMIDES

A series of novel 4-amino-2-(thiadiazole-carbonyl piperazinyl)-6,7-dimethoxyquinazolines is disclosed having antihypertensive properties. The thiadiazole substituent may be optionally substituted with alkyl or lower alkoxy carbonylamino groups. A representative embodiment of the invention is 4-amino-6,7-dimethoxy-2-4-(5-ethoxy-carbonylamino-1,2,3-thiadiazole-4-carbonyl)-piperazin-1-yl!-qui nazoline.