10550-15-9 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
3-(4-chlorophenyl)-1,2,4-oxadiazole serves as a key building block for the synthesis of various pharmaceutical and agrochemical products due to its versatile reactivity and the ability to be easily functionalized. Its incorporation into these products can enhance their therapeutic or pesticidal efficacy.
Used in Antiviral, Antitumor, and Antimicrobial Applications:
3-(4-chlorophenyl)-1,2,4-oxadiazole is utilized in the development of antiviral, antitumor, and antimicrobial agents because of its potential biological activities. Its presence in drug molecules can contribute to their effectiveness against viruses, tumors, and microorganisms.
Used in Optoelectronic Materials Development:
Owing to its luminescent properties, 3-(4-chlorophenyl)-1,2,4-oxadiazole is applied in the creation of materials for optoelectronic applications. Its light-emitting characteristics can be harnessed in the design of devices such as organic light-emitting diodes (OLEDs) and other optoelectronic components.
Used in Research and Development:
3-(4-chlorophenyl)-1,2,4-oxadiazole is a subject of ongoing research in the fields of organic chemistry, materials science, and medicinal chemistry. Its unique properties and potential applications make it an interesting compound for scientists to explore and innovate further uses and syntheses.
Check Digit Verification of cas no
The CAS Registry Mumber 10550-15-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,5 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10550-15:
(7*1)+(6*0)+(5*5)+(4*5)+(3*0)+(2*1)+(1*5)=59
59 % 10 = 9
So 10550-15-9 is a valid CAS Registry Number.
10550-15-9Relevant academic research and scientific papers
Palladium-Catalyzed, Silver-Assisted Direct C-5–H Arylation of 3-Substituted 1,2,4-Oxadiazoles under Microwave Irradiation
Li, Shan,Wan, Penghui,Ai, Jing,Sheng, Rong,Hu, Yongzhou,Hu, Youhong
supporting information, p. 772 - 778 (2017/03/11)
A direct C-5–H arylation of 3-substituted 1,2,4-oxadiazoles with aryl iodides in the presence of a palladium catalyst and silver acetate is reported. This method provides a rapid, reliable way to obtain versatile 3,5-diaryl-1,2,4-oxadiazole derivatives, which are common moieties of many biologically active molecules. The synthetic applications of this novel method have been demonstrated in the concise syntheses of Ataluren and a potent RET inhibitor Yhhu251. (Figure presented.).
Iron(III) Chloride/l-Proline as an Efficient Catalyst for the Synthesis of 3-Substituted 1,2,4-Oxadiazoles from Amidoximes and Triethyl Orthoformate
Kaboudin, Babak,Kazemi, Foad,Pirouz, Maryam,Khoshkhoo, Aysan Baharian,Kato, Jun-Ya,Yokomatsu, Tsutomu
, p. 3597 - 3602 (2016/10/18)
A general, facile, and efficient method is presented for the synthesis of 3-substituted 1,2,4-oxadiazoles from amidoximes and triethyl orthoformate. The procedure employs an iron(III) chloride/l-proline catalytic system and the 3-substituted 1,2,4-oxadiaz
SYNTHESIS OF TRIAZOLES AND OXADIAZOLES FROM 2-ARYL-3-PHENYL-4-IMINO-5-CYANO-3,4-DIHYDROPYRIMIDINES
Robev, Stefan K.
, p. 2903 - 2906 (2007/10/02)
2-Aryl-3-phenyl-4-imino-5-cyano-3,4-dihydropyrimidines I were transformed to 1,2,4-triazoles II,IV and 1,2,4-oxadiazoles III by treatment with hydrazine, arylhydrazines or hydroxylamine in yields up to 90percent.
