40753-14-8 Usage
Description
4-(4-METHYLPHENYL)-1,2,3-THIADIAZOLE is a chemical compound belonging to the thiadiazole class, characterized by a thiadiazole ring with a 4-methylphenyl group attached. This unique structure endows it with potential applications across various fields, including pharmaceuticals, agrochemicals, and materials science, making it a valuable building block for synthesizing new compounds with possible biological activity or material properties.
Uses
Used in Pharmaceutical Industry:
4-(4-METHYLPHENYL)-1,2,3-THIADIAZOLE is used as a key intermediate in the synthesis of pharmaceutical compounds for its potential biological activity. Its unique structure allows for the development of new drugs with therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical field, 4-(4-METHYLPHENYL)-1,2,3-THIADIAZOLE is utilized as a building block for the creation of agrochemicals, such as pesticides and herbicides, due to its potential to enhance the effectiveness of these products.
Used in Materials Science:
4-(4-METHYLPHENYL)-1,2,3-THIADIAZOLE is employed in materials science for the development of new materials with specific properties. Its unique structure contributes to the creation of materials with potential applications in various industries.
Further research and exploration of 4-(4-METHYLPHENYL)-1,2,3-THIADIAZOLE's potential applications are ongoing, indicating its significance in the scientific community for future advancements in these fields.
Check Digit Verification of cas no
The CAS Registry Mumber 40753-14-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,7,5 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 40753-14:
(7*4)+(6*0)+(5*7)+(4*5)+(3*3)+(2*1)+(1*4)=98
98 % 10 = 8
So 40753-14-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H8N2S/c1-7-2-4-8(5-3-7)9-6-12-11-10-9/h2-6H,1H3
40753-14-8Relevant articles and documents
Synthesis method of 1, 2, 3-thiadiazole derivative
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Paragraph 0109-0142, (2021/08/28)
The invention belongs to the technical field of compound preparation, and discloses a synthesis method of a 1, 2, 3-thiadiazole derivative. The synthesis method of the 1, 2, 3-thiadiazole derivative comprises the following steps: taking an N-tosylhydrazon
Diiiodine/Potassium Persulfate Mediated Synthesis of 1,2,3-Thiadiazoles from N -Tosylhydrazones and a Thiocyanate Salt as a Sulfur Source under Transition-Metal-Free Conditions
Lu, Yuhan,Sun, Yadong,Abdukader, Ablimit,Liu, Chenjiang
supporting information, p. 1044 - 1048 (2021/05/05)
A highly efficient method for the synthesis of 1,2,3-thiadiazoles has been developed by utilizing readily available tosylhydrazones and ammonium thiocyanate with ecofriendly EtOH as the solvent at room temperature. The reaction shows a wide scope of subst
I2/CuCl2-promoted one-pot three-component synthesis of aliphatic or aromatic substituted 1,2,3-thiadiazoles
Wang, Can,Geng, Xiao,Zhao, Peng,Zhou, You,Wu, Yan-Dong,Cui, Yan-Fang,Wu, An-Xin
supporting information, p. 8134 - 8137 (2019/07/15)
An efficient I2/CuCl2-promoted one-pot three-component strategy for the construction of 1,2,3-thiadiazoles from aliphatic- or aromatic-substituted methyl ketones, p-toluenesulfonyl hydrazide, and potassium thiocyanate has been develo
