1925-79-7 Usage
Thiadiazole family
Five-membered ring with three nitrogen and two sulfur atoms
The compound belongs to a family of compounds with a specific ring structure containing nitrogen and sulfur atoms.
Ethylthio group
An ethyl group (CH2CH3) attached to a sulfur atom
The compound features an ethylthio group, which is a sulfur atom bonded to an ethyl group.
Methyl group
A single carbon atom (CH3) attached to the thiadiazole ring
The compound also contains a methyl group, which is a single carbon atom with three hydrogen atoms bonded to the thiadiazole ring.
Pharmaceutical industry
Used as a building block for the synthesis of biologically active compounds
The compound is utilized in the pharmaceutical industry to create various compounds with potential applications in medicine, such as fungicides and herbicides.
Organic synthesis
Valuable intermediate in the synthesis of other organic compounds
Due to its unique structure and chemical properties, the compound serves as an important intermediate in the synthesis of other organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 1925-79-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,2 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1925-79:
(6*1)+(5*9)+(4*2)+(3*5)+(2*7)+(1*9)=97
97 % 10 = 7
So 1925-79-7 is a valid CAS Registry Number.
1925-79-7Relevant academic research and scientific papers
Gogoi, Robin,Kumar, Rajesh,Pal, Suprabhat,Singh, Vikrant
, (2020)
Being the important organic reaction intermediates and biological scaffolds, a series of 2-alkyl/aralkyl/heterocyclyl sulfanyl-5-amino/methyl-1,3,4-thiadiazoles have been synthesized by suitable synthetic route and characterized by analytical and spectral data. The evaluation of these compounds for their bioefficacy against two phyto-pathogenic fungi revealed their fungicidal potency against Rhizoctonia bataticola (ED50 values, 3.9–300.4 μg/mL) and Rhizoctonia solani (ED50 values, 4.2–228.5 μg/mL). To further augment their fungicidal efficacy, the potent five fungicidal compounds were nano-sized. The protocol for preparing 1,3,4-thiadiazole based nano-fungicide employing polyethylene glycol was developed and standardized. Characterization of nano-forms of 1,3,4-thiadiazole derivatives by particle size analyzer and electron microscopy (TEM) techniques confirmed the 100 nm average particle sizes of all nano-fungicides. The 2–4 times higher fungicidal activity was observed with nano-forms than the corresponding conventional sized 1,3,4-thiadiazole derivatives against phytopathogenic fungi, namely, Rhizoctonia solani and R. bataticola.
