83629-96-3 Usage
Chemical structure
Ketone derivative with a quinoline ring and a propyl moiety
The compound has a carbonyl group (C=O) attached to a quinoline ring, which is a tricyclic aromatic system, and a propyl group (C3H7) attached to the carbonyl carbon.
Synonyms
N-Quinolin-4-ylpropan-1-one
This is an alternative name for the compound, highlighting the presence of a quinoline ring at the 4-position and a propyl group attached to the carbonyl carbon.
Applications
Building block in the synthesis of pharmaceuticals and other organic compounds
Due to its unique structure, 1-(quinolin-4-yl)propan-1-one is used as an intermediate in the synthesis of various pharmaceuticals and organic compounds, making it a versatile chemical.
Biological activities
Potential as an antifungal and antibacterial agent
Studies have shown that 1-(quinolin-4-yl)propan-1-one may have potential applications in the field of medicine, particularly as an antifungal and antibacterial agent.
Fields of application
Medicine and materials science
The compound's versatility and potential biological activities make it applicable in various fields, including the development of new drugs and materials with specific properties.
Solubility
Soluble in organic solvents
As an organic compound, 1-(quinolin-4-yl)propan-1-one is generally soluble in organic solvents such as ethanol, methanol, and acetone, which is important for its use in chemical reactions and purification processes.
Stability
Stable under normal conditions
The compound is considered stable under normal laboratory conditions, making it suitable for use in various chemical reactions and applications.
Melting point
Not provided in the material
The melting point of 1-(quinolin-4-yl)propan-1-one is not mentioned in the provided material, but it is an important physical property that can be determined experimentally.
Boiling point
Not provided in the material
Similarly, the boiling point of the compound is not provided in the material, but it is another important physical property that can be determined through experimentation.
Check Digit Verification of cas no
The CAS Registry Mumber 83629-96-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,6,2 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 83629-96:
(7*8)+(6*3)+(5*6)+(4*2)+(3*9)+(2*9)+(1*6)=163
163 % 10 = 3
So 83629-96-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H11NO/c1-2-12(14)10-7-8-13-11-6-4-3-5-9(10)11/h3-8H,2H2,1H3
83629-96-3Relevant articles and documents
Transition-Metal-Free Oxidation of Benzylic C-H Bonds of Six-Membered N-Heteroaromatic Compounds
Gao, Xianying,Han, Shuaijun,Zheng, Maolin,Liang, Apeng,Zou, Dapeng,Wu, Yusheng,Wu, Yangjie,Li, Jingya
, p. 4040 - 4049 (2019/04/30)
A novel oxidation of benzylic C-H bonds for the synthesis of diverse six-membered N-heteroaromatic aldehydes and ketones has been developed. The obvious advantages of this approach are the simple operation, mild reaction conditions, and without use of toxic reagent and transition metal. The present method should provide a useful access for the synthesis and modification of N-heterocycles.
Homolytic Acylation of Protonated Pyridines and Pyrazines with α-Keto Acids: The Problem of Monoacylation
Fontana, Francesca,Minisci, Francesco,Barbosa, Maria Claudia Nogueira,Vismara, Elena
, p. 2866 - 2869 (2007/10/02)
The silver-catalyzed decarboxylation of α-keto acids by persulfate leads to acyl radicals, which can effect the selective homolytic acylation of pyridine and pyrazine derivatives.Compared with the previously developed source of acyl radicals by hydrogen abstraction from aldehydes, this procedure is more effective in monoacylation when multiple positions of high nucleophilic reactivity are available in the heterocyclic ring.Although the introduction of an acyl group strongly activates the heterocyclic ring toward further substitution, monoacylation can be achieved by taking advantage of the difference in basicity and lipophilicity between the starting base and the monoacylation products in a two-phase system.
