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.
Check Digit Verification of cas no
The CAS Registry Mumber 54742-57-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,7,4 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 54742-57:
(7*5)+(6*4)+(5*7)+(4*4)+(3*2)+(2*5)+(1*7)=133
133 % 10 = 3
So 54742-57-3 is a valid CAS Registry Number.
54742-57-3Relevant articles and documents
Preparation and promotion of fruit growth in kiwifruit of fluorinated N-phenyl-N′-1,2,3-thiadiazol-5-yl ureas
Abad, Antonio,Agullo, Consuelo,Cunat, Ana Carmen,Jimenez, Raquel,Vilanova, Cristina
, p. 4675 - 4683 (2004)
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
Method of treating a patient having precancerous lesions with quinazoline derivatives
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, (2008/06/13)
Derivatives of Quinazoline are useful for the treatment of patients having precancerous lesions. These compounds are also useful to inhibit growth of neoplastic cells.
Selenium heterocycles XVIII: synthesis and antibacterial activity of 4 substituted (1,2,3 selenadiazol 5 yl)carbamic acid esters and their sulfur analogs
Shafiee,Lalezari,Yazdani,Shahbazian,Partovi
, p. 304 - 307 (2007/10/08)
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