144603-01-0 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
The compound is derived from the quinoline structure, which is a tricyclic aromatic compound.
Explanation
The presence of a hydroxy group (-OH) and two ethyl groups (-CH2CH3) attached to the quinoline structure.
Explanation
The compound can help prevent oxidative damage by scavenging free radicals, which are unstable molecules that can cause cellular damage.
Explanation
The compound can form stable complexes with metal ions, which can be useful in various industrial and pharmaceutical applications.
Explanation
Due to its unique chemical structure, the compound can be used as a starting material for the production of other chemicals and pharmaceutical drugs.
Explanation
The compound's unique chemical structure and potential medicinal properties make it a valuable component in the development of drugs for treating malaria and cancer.
Explanation
The compound is likely to dissolve in organic solvents such as ethanol, methanol, or acetone, which can be important for its use in chemical reactions and pharmaceutical formulations.
Explanation
The compound is expected to be stable at room temperature and in the absence of strong acids, bases, or oxidizing agents.
Explanation
As with many chemicals, the compound may have toxic effects if ingested, inhaled, or absorbed through the skin in large quantities or over an extended period. However, its use in pharmaceutical applications suggests that it can be safely used in controlled doses.
Chemical structure
Quinoline derivative
Functional groups
Hydroxy group and two ethyl substituents
Antioxidant properties
Capable of neutralizing free radicals
Chelating properties
Ability to bind to metal ions
Industrial applications
Used as an intermediate in the synthesis of other chemicals
Pharmaceutical applications
Used in the production of antimalarial and antitumor drugs
Solubility
Generally soluble in organic solvents
Stability
Relatively stable under normal conditions
Toxicity
Potential for toxicity depending on dosage and exposure
Check Digit Verification of cas no
The CAS Registry Mumber 144603-01-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,6,0 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 144603-01:
(8*1)+(7*4)+(6*4)+(5*6)+(4*0)+(3*3)+(2*0)+(1*1)=100
100 % 10 = 0
So 144603-01-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H15NO2/c1-3-9-12(15)10-7-5-6-8-11(10)14(4-2)13(9)16/h5-8,16H,3-4H2,1-2H3
144603-01-0Relevant articles and documents
Halogenation Reactions in Position 3 of Quinoline-2,4-dione Systems by Electrophilic Substitution and Halogen Exchange
Stadlbauer, Wolfgang,Laschober, Rita,Lutschounig, Herbert,Schindler, Gerda,Kappe, Thomas
, p. 617 - 636 (2007/10/02)
3-Substituted 4-hydroxy-2(1H)-quinolones 3, 5, 7 are halogenated with bromine or sulfuryl chloride to yield the quinolinediones 9 or 10.Reactions of 3, 5, 7 with chloroform gives the dichloromethyl quinolinediones 11.Halogen exchange leads from the chloro quinolinediones 10 to fluoro quinolinedones 12 and to azido quinolinediones 13.Similarly the dichloro quinolinediones 10an reacts to the difluoro quinolinedione 14, which is reduced to the 3-fluoro-4-hydroxyquinolone 16 and reacts again with sulfuryl chloride to give the mixed 3-chloro-3-fluoroquinolinedione 15.Keywords.Fluorination; 4-Hydroxy-2(1H)-quinolones, 3-alkyl/3-aryl/3-fluoro; 1-Hydroxy-benzoquinolizine-3-ones, 2-alkyl/3-aryl; Quinoline-2,4(1H,3H)-diones, 3-azido-3-alkyl/3-aryl, 3-bromo-3-alkyl/3-aryl, 3-chloro-3-alkyl/3-aryl, 3-fluoro-3-alkyl/3-aryl, 3-dichloromethyl-3-alkyl/3-aryl, 3-chloro-3-fluoro.
