944905-96-8 Usage
Uses
Used in Pharmaceutical Applications:
3-[4-(trifluoromethyl)phenyl]-1,2,4-oxadiazol-5-ylmethanamine is used as a monoamine oxidase inhibitor for the treatment of neurological disorders such as depression and anxiety. Its ability to inhibit monoamine oxidase enzymes can help regulate the levels of neurotransmitters in the brain, providing relief from the symptoms of these conditions.
Additionally, the presence of fluorine substituents in the compound may offer certain advantages in medicinal chemistry, such as improved pharmacokinetic properties or enhanced binding affinity to target proteins. However, further research and testing are necessary to fully understand the compound's biological activity and its potential as a therapeutic agent.
Used in Medicinal Chemistry Research:
3-[4-(trifluoromethyl)phenyl]-1,2,4-oxadiazol-5-ylmethanamine can be utilized as a starting material or a structural motif in the design and synthesis of new pharmaceutical compounds. Its unique properties, including the presence of the trifluoromethyl group and the oxadiazole ring, may provide a foundation for the development of novel drugs with improved efficacy, selectivity, and safety profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 944905-96-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,4,9,0 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 944905-96:
(8*9)+(7*4)+(6*4)+(5*9)+(4*0)+(3*5)+(2*9)+(1*6)=208
208 % 10 = 8
So 944905-96-8 is a valid CAS Registry Number.
944905-96-8Relevant articles and documents
Design, synthesis, and biological activities of novel 2-cyanoacrylates containing oxazole, oxadiazole, or quinoline moieties
Zhao, Qiqi,Liu, Shaohua,Li, Yonghong,Wang, Qingmin
experimental part, p. 2849 - 2855 (2010/04/30)
A series of novel 2-cyanoacrylates containing an oxazole, oxadiazole, or quinoline moiety were designed and synthesized, and their structures were characterized by 1H NMR and elemental analysis (or high-resolution mass spectrometry). Their herbicidal activities against four weeds were evaluated, and the result indicated that some of the title compounds showed excellent herbicidal activities against rape and amaranth pigweed in postemergence treatment at a dose of 375 g/ha. Furthermore, most of these cyanoacrylates exhibited interesting plant growth regulatory activities.
