19922-07-7 Usage
Uses
Used in Research and Development:
5-Amino-3-(4-chlorophenyl)-1,2,4-thiadiazole is used as a chemical intermediate for the synthesis of various compounds in the field of organic chemistry. Its unique structure, including the thiadiazole ring and the chlorine-substituted phenyl group, makes it a candidate for further exploration in chemical reactions and potential applications.
Used in Pharmaceutical Industry:
5-Amino-3-(4-chlorophenyl)-1,2,4-thiadiazole is used as a building block in the development of new pharmaceutical compounds. The presence of the amino group and the heterocyclic thiadiazole ring may offer opportunities for the creation of novel drug molecules with potential therapeutic applications.
Used in Material Science:
5-Amino-3-(4-chlorophenyl)-1,2,4-thiadiazole is used as a component in the synthesis of advanced materials, such as organic semiconductors or functional polymers. 5-Amino-3-(4-chlorophenyl)-1,2,4-thiadiazole's reactivity and structural features may contribute to the development of new materials with specific properties for various applications.
Used in Agrochemical Industry:
5-Amino-3-(4-chlorophenyl)-1,2,4-thiadiazole is used as a precursor in the synthesis of agrochemicals, such as pesticides or herbicides. 5-Amino-3-(4-chlorophenyl)-1,2,4-thiadiazole's reactivity and structural features may be exploited to create new active ingredients with improved efficacy and selectivity in agricultural applications.
Used in Dye and Pigment Industry:
5-Amino-3-(4-chlorophenyl)-1,2,4-thiadiazole is used as a starting material for the production of dyes and pigments. 5-Amino-3-(4-chlorophenyl)-1,2,4-thiadiazole's structural features may be utilized to develop new colorants with enhanced properties, such as improved color strength, stability, or solubility.
Check Digit Verification of cas no
The CAS Registry Mumber 19922-07-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,2 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 19922-07:
(7*1)+(6*9)+(5*9)+(4*2)+(3*2)+(2*0)+(1*7)=127
127 % 10 = 7
So 19922-07-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H6ClN3S/c9-6-3-1-5(2-4-6)7-11-8(10)13-12-7/h1-4H,(H2,10,11,12)
19922-07-7Relevant academic research and scientific papers
One-Pot Synthesis of 3-Aryl-5-amino-1,2,4-thiadiazoles from Imidates and Thioureas by I2-Mediated Oxidative Construction of the N–S Bond
Chai, Ling,Lai, Zhenzhen,Xia, Qiangqiang,Yuan, Jiangpei,Bian, Qilong,Yu, Mingjian,Zhang, Wenkai,Xu, Yuanqing,Xu, Hao
, p. 4338 - 4344 (2018/08/31)
A simple and practical method for the one-pot synthesis of 3-aryl-5-amino-1,2,4-thiadiazoles from imidates and thioureas has been developed. The protocol proceeds through sequential base-mediated nucleophilic addition-elimination reactions and an I2-mediated oxidative coupling for the N–S bond formation. The approach employes readily available and nontoxic substrates and a simple workup to provide 3-aryl-5-amino-1,2,4-thiadiazoles that have a free or substituted amino group.
