3914-44-1 Usage
Uses
Used in Pharmaceutical Industry:
2-(Chloromethyl)-5-methoxy-1,3,4-thiadiazole is used as a building block for the synthesis of pharmaceuticals, contributing to the development of new drugs. Its unique structure allows for the creation of bioactive molecules with potential therapeutic applications.
Used in Agrochemical Industry:
2-(Chloromethyl)-5-methoxy-1,3,4-thiadiazole is used as a building block for the synthesis of agrochemicals, such as pesticides and herbicides. Its properties enable the development of effective compounds for agricultural use, enhancing crop protection and yield.
Used in Drug Discovery Research:
2-(Chloromethyl)-5-methoxy-1,3,4-thiadiazole is used as a research compound in the field of drug discovery. Its potential biological activities and pharmacological properties make it a valuable tool for exploring new therapeutic avenues and understanding the mechanisms of action of various drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 3914-44-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,1 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3914-44:
(6*3)+(5*9)+(4*1)+(3*4)+(2*4)+(1*4)=91
91 % 10 = 1
So 3914-44-1 is a valid CAS Registry Number.
3914-44-1Relevant academic research and scientific papers
Synthesis and biological activities of novel 1,3,4-thiadiazole-containing pyrazole oxime derivatives
Dai, Hong,Li, Gang,Chen, Jia,Shi, Yujun,Ge, Shushan,Fan, Chongguang,He, Haibing
supporting information, p. 3818 - 3821 (2016/07/21)
A new library of 1,3,4-thiadiazole-containing pyrazole oximes was designed and synthesized. Their acaricidal and insecticidal activities were evaluated. Bioassay results indicated that some target compounds exhibited good acaricidal and insecticidal properties. Especially, compound 8m had 80% acaricidal activity against Tetranychus cinnabarinus at the concentration of 50?μg/mL, compound 8f displayed 100% insecticidal activities against Aphis craccivora at the concentration of 50?μg/mL, compounds 8r and 8w showed 100% insecticidal activities against Plutella xylostella at the concentration of 50?μg/mL. Furthermore, compounds 8r (LC50?=?19.61?μg/mL) and 8w (LC50?=?9.78?μg/mL) possessed comparable or even better insecticidal activities than the control Pyridalyl (LC50?=?17.40?μg/mL) against P. xylostella.
