696604-74-7 Usage
Uses
Used in Pharmaceutical Industry:
2-(CHLOROMETHYL)-5-(3,4-DIMETHOXYPHENYL)-1,3,4-OXADIAZOLE is utilized as a key intermediate in the synthesis of pharmaceuticals due to its antimicrobial, anticancer, and anti-inflammatory properties. Its diverse biological activities make it a promising candidate for the development of new drugs with enhanced efficacy and reduced side effects.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(CHLOROMETHYL)-5-(3,4-DIMETHOXYPHENYL)-1,3,4-OXADIAZOLE serves as a vital component in the creation of novel agrochemicals. Its potential applications include the development of pesticides with improved effectiveness against various pests and diseases, while also aiming to minimize the environmental impact associated with traditional agrochemicals.
2-(CHLOROMETHYL)-5-(3,4-DIMETHOXYPHENYL)-1,3,4-OXADIAZOLE's reactivity and structural features also make it a valuable asset for further research, with the potential to uncover additional applications and properties that could contribute to advancements in both the pharmaceutical and agrochemical fields.
Check Digit Verification of cas no
The CAS Registry Mumber 696604-74-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,6,6,0 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 696604-74:
(8*6)+(7*9)+(6*6)+(5*6)+(4*0)+(3*4)+(2*7)+(1*4)=207
207 % 10 = 7
So 696604-74-7 is a valid CAS Registry Number.
696604-74-7Relevant academic research and scientific papers
Synthesis and antimicrobial properties of 1,3,4-oxadiazole analogs containing dibenzosuberane moiety
Moger, Manjunath,Satam, Vijay,Govindaraju, Darshan Raj C.,Paniraj,Gopinath, Vadiraj S.,Hindupur, Rama Mohan,Pati, Hari N.
, p. 104 - 111 (2014/02/14)
A series of ten novel 1,3,4-oxadiazole analogs containing dibenzosuberane moiety were synthesized using linear as well as convergent synthesis approach. All the compounds were characterized by mass spectrometry, infrared (IR), 1H and 13C nuclear magnetic resonance (1H NMR and 13C NMR) spectroscopies and elemental analysis. These compounds were evaluated for antibacterial and antifungal activities. Among ten analogs, four compounds, namely, 8a, 8d, 8e and 8j were found to be highly active antibacterial and antifungal agents.
