179056-82-7 Usage
Description
4-(5-METHYL-1,2,4-OXADIAZOL-3-YL)BENZALDEHYDE is a chemical compound characterized by its molecular formula C9H7N3O2. It is a yellow crystalline solid with a molecular weight of 193.17 g/mol. 4-(5-METHYL-1,2,4-OXADIAZOL-3-YL)BENZALDEHYDE is utilized in various fields, particularly in organic synthesis and pharmaceutical research, where it serves as a building block for the creation of diverse organic molecules. Additionally, it has been the subject of studies exploring its potential biological activities and pharmacological properties, indicating its versatility and importance in scientific research and development.
Uses
Used in Organic Synthesis:
4-(5-METHYL-1,2,4-OXADIAZOL-3-YL)BENZALDEHYDE is used as a building block in organic synthesis for the creation of various organic molecules. Its unique structure allows it to be a valuable component in the formation of complex organic compounds, contributing to the advancement of chemical research and the development of new materials.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4-(5-METHYL-1,2,4-OXADIAZOL-3-YL)BENZALDEHYDE is used as a building block for the development of new drugs. Its potential biological activities and pharmacological properties make it a promising candidate for the creation of innovative therapeutic agents, potentially leading to breakthroughs in medicine.
Used in Research and Development:
4-(5-METHYL-1,2,4-OXADIAZOL-3-YL)BENZALDEHYDE is utilized in research and development across various industries. Its specific applications may vary depending on the needs and objectives of the research, but its potential for contributing to scientific advancements is evident. 4-(5-METHYL-1,2,4-OXADIAZOL-3-YL)BENZALDEHYDE's role in the discovery and development of new technologies and products is significant, as it can be adapted to meet the demands of different fields.
Check Digit Verification of cas no
The CAS Registry Mumber 179056-82-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,0,5 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 179056-82:
(8*1)+(7*7)+(6*9)+(5*0)+(4*5)+(3*6)+(2*8)+(1*2)=167
167 % 10 = 7
So 179056-82-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H8N2O2/c1-7-11-12-10(14-7)9-4-2-8(6-13)3-5-9/h2-6H,1H3
179056-82-7Relevant articles and documents
Palladium-Catalyzed Reductive Carbonylation of (Hetero) Aryl Halides and Triflates Using Cobalt Carbonyl as CO Source
Dogga, Bhushanarao,Joseph, Jayan T.,Kumar, C. S. Ananda
, p. 309 - 313 (2020/12/23)
An efficient protocol for the reductive carbonylation of (hetero) aryl halides and triflates under CO gas-free conditions using Pd/Co2(CO)8 and triethylsilane has been developed. The mild reaction conditions, enhanced chemoselectivity and, easy access to heterocyclic and vinyl carboxaldehydes highlights its importance in organic synthesis.