59834-07-0 Usage
Uses
Used in Pharmaceutical Applications:
4-[4-(Oxiran-2-ylmethoxy)phenyl]-1,2,3-thiadiazole is used as a potential antimicrobial, anticancer, and antioxidant agent due to its unique chemical structure and reactivity. The presence of the oxiran-2-ylmethoxy group may enhance the compound's biological activities, making it a candidate for the development of new therapeutic agents.
Used in Materials Science:
In the field of materials science, 4-[4-(oxiran-2-ylmethoxy)phenyl]-1,2,3-thiadiazole is used in the development of organic electronics and fluorescent probes. Its unique electronic and optical properties make it suitable for these applications, where it can contribute to the advancement of technology in these areas.
Used in Organic Electronics Industry:
4-[4-(Oxiran-2-ylmethoxy)phenyl]-1,2,3-thiadiazole is used as a component in organic electronic devices for its electronic properties, which can improve the performance and functionality of these devices.
Used in Fluorescent Probes Development:
In the development of fluorescent probes, 4-[4-(oxiran-2-ylmethoxy)phenyl]-1,2,3-thiadiazole is used as a component that can enhance the optical properties of the probes, making them more sensitive and specific for various analytical applications.
Further research on 4-[4-(oxiran-2-ylmethoxy)phenyl]-1,2,3-thiadiazole could reveal additional applications for 4-[4-(OXIRAN-2-YLMETHOXY)PHENYL]-1,2,3-THIADIAZOLE in different fields, expanding its utility and potential impact on various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 59834-07-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,8,3 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 59834-07:
(7*5)+(6*9)+(5*8)+(4*3)+(3*4)+(2*0)+(1*7)=160
160 % 10 = 0
So 59834-07-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H10N2O2S/c1-3-9(14-5-10-6-15-10)4-2-8(1)11-7-16-13-12-11/h1-4,7,10H,5-6H2
59834-07-0Relevant academic research and scientific papers
Synthesis, antimicrobial and in vitro antitumor activities of a series of 1,2,3-thiadiazole and 1,2,3-selenadiazole derivatives
Mhaidat, Nizar M.,Al-Smadi, Mousa,Al-Momani, Fouad,Alzoubi, Karem H.,Mansi, Iman,Al-Balas, Qosay
, p. 3645 - 3652 (2015/08/03)
Three derivatives of substituted 1,2,3-thia- or 1,2,3-selenadiazole (4ac) were prepared and characterized by different chemical techniques. These compounds were evaluated for their antimicrobial and antitumor activities. Compounds 4a (propenoxide derivati
1,2,3-Thiadiazoles with unsaturated side chains; synthesis, polymerization, and photocrosslinking
Al-Smadi, Mousa,Hanold, Norbert,Kalbitz, Helga,Meier, Herbert
experimental part, p. 2539 - 2546 (2009/12/08)
1,2,3-Thiadiazoles with polymerizable functionalities in the 4-position were synthesized as potential negative photoresists. The polymerization to soluble, film-forming materials must leave the heterocyclic rings intact, because they are needed for photocrosslinking reactions to give insoluble materials. 1,2,3-Thiadiazoles 1 cycloeliminate N2 on irradiation. The resulting 1,3-diradicals 2 have various options for stabilization processes leading to alkynes 3 or to higher heterocycles 5-12. The generation of atomic sulfur and its involvement in these subsequent reactions must be avoided. Therefore, systems like model compound 1a, in which the 1,3-diradicals form 2-methylene-1,3-dithioles (dithiafulvenes) 9 were selected here. Optimization gave ultimately two materials for application as photoresists. Monomer 1c could be polymerized in the presence of boron trifluoride to soluble 1c′, which on irradiation formed 1c″ as a cross-linked insoluble polymer. Furthermore, thiadiazole 1f was attached to polystyrene 26. The resulting soluble polymer 1i′ yielded the insoluble material 1i″ on irradiation. Georg Thieme Verlag Stuttgart.
