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2-(Phenylthio)-1,3,4-thiadiazole is a chemical compound with the molecular formula C7H4N2S3. It is a heterocyclic compound, specifically a thiadiazole derivative, which features a five-membered ring containing three sulfur atoms and two nitrogen atoms. The phenylthio group is attached to the 2-position of the thiadiazole ring, providing a phenyl ring connected to the sulfur atom. 2-(phenylthio)-1,3,4-thiadiazole is known for its potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science, due to its unique chemical properties and reactivity. It can be synthesized through various methods, including the reaction of phenyl isothiocyanate with 1,3,4-thiadiazole-2-thiol, and is often used as a building block for the development of more complex molecules with specific functionalities.

3530-72-1

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3530-72-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3530-72-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,3 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3530-72:
(6*3)+(5*5)+(4*3)+(3*0)+(2*7)+(1*2)=71
71 % 10 = 1
So 3530-72-1 is a valid CAS Registry Number.

3530-72-1Downstream Products

3530-72-1Relevant academic research and scientific papers

Efficient formation of C–S bond using heterocyclic thiones and arynes

An, Yu,Xu, Gang,Cai, Menglu,Wang, Shihui,Wang, Xiao zhong,Chen, Yingqi,Dai, Liyan

, (2021)

Phenylthio heterocyclic compounds are widely used because of their diverse biological activities and medicinal prospects. Here, a facile method was reported. An arylation of 1,3,4-oxa(thia)diazol-2-thiones reacting with arynes to build C(aryl)-S bonds in the presence of CsF had good yields and excellent selectivity. The reaction was completed in short time without using expensive reagents and catalysts. Present reaction system is an efficient procedure to process phenylthio heterocyclic compounds and reveals a sustainable method and better application prospects in future organic synthesis.

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