33459-12-0 Usage
Nitrobenzoic acid derivative
A derivative of nitrobenzoic acid This indicates that the compound is structurally related to nitrobenzoic acid, with modifications to the parent molecule.
Methoxyphenyl group
Presence of a methoxy group attached to a phenyl ring This functional group contributes to the compound's chemical properties and reactivity.
Nitro group
Presence of a nitro group (-NO2) This functional group is known for its reactivity and can be involved in various chemical reactions.
Common use in synthesis
Used in the synthesis of pharmaceuticals and agrochemicals This highlights the compound's potential applications in creating various products with biological and therapeutic activities.
Building block in organic synthesis
Can be used as a starting material for further chemical reactions This property makes it valuable in the field of organic chemistry for creating more complex molecules.
Antioxidant properties
Potential to neutralize free radicals and prevent oxidative damage This makes the compound of interest in the development of treatments for various diseases and conditions related to oxidative stress.
Anti-inflammatory properties
Potential to reduce inflammation and alleviate symptoms of inflammatory conditions This adds to the compound's potential therapeutic applications in the field of medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 33459-12-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,4,5 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 33459-12:
(7*3)+(6*3)+(5*4)+(4*5)+(3*9)+(2*1)+(1*2)=110
110 % 10 = 0
So 33459-12-0 is a valid CAS Registry Number.
33459-12-0Relevant articles and documents
Synthesis and anticoccidial activities of substituted ethyl 4-hydroxy-11-oxo-11H-chromeno[2,3-g]quinoline-3-carboxylates
Wang, Zhi,Zhou, Li-Juan,Wang, Yu-Liang,Weng, Ya-Biao,He, Jun,Nie, Kui
experimental part, p. 373 - 376 (2011/10/02)
A series of substituted ethyl 4-hydroxy-11-oxo-11H-chromeno[2,3-g] quinoline-3-carboxylates were designed and synthesised as anticoccidial drugs, and the structures were characterised by 1H NMR, MS, IR spectra and elementary analysis. The antic
