18465-39-9 Usage
Molecular structure
A complex structure containing a quinoline ring system, a carboxylic acid group, and hydroxy and oxo functional groups.
Quinoline ring system
A core structure consisting of a fused 4-six-membered ring system, which contributes to the compound's potential biological activity.
Carboxylic acid group
A functional group (-COOH) attached to the quinoline ring, which may contribute to the compound's potential for chelation and metal-binding properties.
Hydroxy and oxo functional groups
These groups (-OH and =O, respectively) are present in the molecule, further contributing to its potential biological activity and reactivity.
Ethyl group
A single carbon chain (-CH2-CH3) attached to the quinoline ring, which may influence the compound's properties and potential applications.
Potential pharmaceutical applications
Due to its structural similarity to quinolone antibiotics, which are known for their antibacterial properties, this compound may have potential pharmaceutical or medicinal applications.
Chelation and metal-binding properties
The presence of hydroxy and carboxylic acid groups suggests that the compound may be able to form complexes with metal ions, which could be useful in various applications.
Biological activity and reactivity
The chemical structure of 1-ethyl-6,7-dihydroxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid indicates that it may have potential for interacting with biological systems and exhibiting various pharmacological effects.
Check Digit Verification of cas no
The CAS Registry Mumber 18465-39-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,6 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 18465-39:
(7*1)+(6*8)+(5*4)+(4*6)+(3*5)+(2*3)+(1*9)=129
129 % 10 = 9
So 18465-39-9 is a valid CAS Registry Number.
18465-39-9Relevant articles and documents
SYNTHESIS AND RADIOPROTECTIVE PROPERTIES OF OXOLINIC ACID DERIVATIVES
Kotel'nikova, N. V.,Leonova, T. S.,Ankudinov, I. V.,Znamenskii, V. V.,Yashunskii, V. G.
, p. 402 - 404 (1991)
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Synthesis and structure-activity relationships of cephalosporins with C-3' catechol-containing residues
Arnould,Bertrandie,Bird,Boucherot,Jung,Lohmann,Olivier,Bailey,Bell,Davies
, p. 2631 - 2642 (2007/10/02)
Cephalosporins with new catechol substituents at C-3' have been synthesized, including novel compounds with C-3' carbon-carbon bonds. Many of these compounds have high potency against Gram-negative bacteria, in particular against resistant strains like Ps
