876935-35-2 Usage
Chemical structure
1,3,4-Oxadiazol-2-amine, N-[4-chloro-3-(trifluoromethyl)phenyl]-5-(1-methyl-4-nitro-1H-imidazol-5-yl)is a complex chemical compound with multiple functional groups.
Functional groups
The compound contains 1,3,4-oxadiazole, chloro-trifluoromethylphenyl, and 1-methyl-4-nitro-1H-imidazol-5-yl groups.
Potential applications
Due to the presence of various functional groups, the compound has potential applications in pharmaceutical and agrochemical industries.
Antimicrobial or antifungal properties
The 5-(1-methyl-4-nitro-1H-imidazol-5-yl) group suggests that the compound may have antimicrobial or antifungal properties.
Further research needed
More research is required to fully understand and utilize the properties of 1,3,4-Oxadiazol-2-amine,
N-[4-chloro-3-(trifluoromethyl)phenyl]-5-(1-methyl-4-nitro-1H-imidazol-5-
yl)- in medicinal and agricultural fields.
Check Digit Verification of cas no
The CAS Registry Mumber 876935-35-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,6,9,3 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 876935-35:
(8*8)+(7*7)+(6*6)+(5*9)+(4*3)+(3*5)+(2*3)+(1*5)=232
232 % 10 = 2
So 876935-35-2 is a valid CAS Registry Number.
876935-35-2Relevant academic research and scientific papers
Hetaryl imidazoles: A novel dual inhibitors of VEGF receptors I and II
Kiselyov, Alexander S.,Semenova, Marina,Semenov, Victor V.
, p. 1440 - 1444 (2007/10/03)
A novel potent derivatives of hetaryl imidazoles were described as inhibitors of vascular endothelial growth factor receptor II (VEGFR-2). Several compounds display VEGFR-2 inhibitory activity reaching IC50 100 nM in both enzymatic and cellular assays. The compounds also inhibit the related tyrosine kinase, VEGFR-1. By controlling the substitution pattern on the 5-carboxamido functionality, both dual and specific VEGFR-2 thiazoles were identified.
