22097-10-5 Usage
General Description
5-Methyl-1,2,3-thiadiazole-4-carboxylic acid is a chemical compound with the molecular formula C5H5N3O2S. It is a heterocyclic compound containing a thiadiazole ring and a carboxylic acid group. 5-Methyl-1,2,3-thiadiazole-4-carboxylic acid is used in the synthesis of pharmaceuticals and agrochemicals, and it has potential applications in the fields of medicine and agriculture. 5-Methyl-1,2,3-thiadiazole-4-carboxylic acid is also used as a building block for the preparation of various derivatives with potential biological activities. Its properties and structure make it a valuable intermediate in organic synthesis and a potential candidate for drug discovery and development.
Check Digit Verification of cas no
The CAS Registry Mumber 22097-10-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,0,9 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 22097-10:
(7*2)+(6*2)+(5*0)+(4*9)+(3*7)+(2*1)+(1*0)=85
85 % 10 = 5
So 22097-10-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H4N2O2S/c1-2-3(4(7)8)5-6-9-2/h1H3,(H,7,8)
22097-10-5Relevant articles and documents
Synthesis and bioactivity of N-tert-butyl-N′-acyl-5-methyl-1,2,3- thiadiazole-4-carbohydrazides
Mao, Wu Tao,Zhao, Hui,Fan, Zhi Jin,Ji, Xiao Tian,Hua, Xue Wen,Kalinina, Tatiana,Yury, Yu. Morzherin,Vasiliy, A. Bakulev
, p. 1233 - 1236,4 (2020/10/15)
A series of novel N-tert-butyl-N′-acyl-5-methyl-1,2,3-thiadiazole-4- carbohydrazides were designed and synthesized. Their structures were characterized by melting points, 1H NMR, IR, ESI-MS, and elemental analysis. The bioassay tests indicated that compound 7o exhibited excellent direct anti-TMV activity and induction activity in vivo at 50 μg/mL, which was better than that of Ninamycin and tiadinial. Our studies indicated that 1,2,3-thiadiazole was an active substructure for novel pesticide development.
