137929-07-8 Usage
Uses
Used in Pharmaceutical Applications:
2-Hydrazino-4-(trifluoromethyl)thiazole is used as a building block for the synthesis of various compounds with potential biological activities. Its unique structure allows for the development of new drugs with specific therapeutic properties.
Used in Agricultural Applications:
In the agricultural industry, 2-Hydrazino-4-(trifluoromethyl)thiazole is used as a building block for the synthesis of compounds with potential pesticidal and herbicidal properties. Its ability to be modified and combined with other chemical groups makes it a valuable component in the development of new agrochemicals.
Used as an Antimicrobial Agent:
2-Hydrazino-4-(trifluoromethyl)thiazole has been studied for its potential use as an antimicrobial agent. Its ability to inhibit the growth of bacteria and other microorganisms makes it a promising candidate for use in various applications, such as in the development of new antibiotics or as a preservative in consumer products.
Used as an Antifungal Agent:
Additionally, 2-Hydrazino-4-(trifluoromethyl)thiazole has been studied for its potential use as an antifungal agent. Its ability to inhibit the growth of fungi can be utilized in the development of new antifungal drugs or in applications such as crop protection and control of fungal infections in various settings.
Check Digit Verification of cas no
The CAS Registry Mumber 137929-07-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,9,2 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 137929-07:
(8*1)+(7*3)+(6*7)+(5*9)+(4*2)+(3*9)+(2*0)+(1*7)=158
158 % 10 = 8
So 137929-07-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H4F3N3S/c5-4(6,7)2-1-11-3(9-2)10-8/h1H,8H2,(H,9,10)
137929-07-8Relevant academic research and scientific papers
Synthesis of Trifluoromethylthiazoles and Their Application to Azo Dyes
Tanaka, Kiyoshi,Nomura, Kazuto,Oda, Hitoshi,Yoshida, Shouhei,Mitsuhashi, Keiryo
, p. 907 - 911 (2007/10/02)
3-Bromo-1,1,1-trifluoropropan-2-one (2) reacted with thiourea and N-monosubstituted thiourea to give the corresponding 4-trifluoromethylthiazoles, respectively.In the reactions with N,N'-diphenylthiourea and thioamides, the considerably stable intermediat
