6480-68-8 Usage
Description
3-Quinolinecarboxylic acid is a quinoline derivative characterized by its antimicrobial properties. It is a white to slightly beige powder, which has been evaluated for its antibacterial activity.
Uses
Used in Pharmaceutical Industry:
3-Quinolinecarboxylic acid is used as an antimicrobial agent for its ability to inhibit the growth of various bacteria. This makes it a valuable compound in the development of new drugs and treatments for bacterial infections.
Used in Research and Development:
In the field of research and development, 3-Quinolinecarboxylic acid serves as a key compound for studying its potential applications in medicine and other industries. Its antimicrobial properties make it an interesting subject for further investigation into its effectiveness against different types of bacteria and possible integration into various products.
Used in Agricultural Industry:
3-Quinolinecarboxylic acid can also be utilized in the agricultural industry as a potential antimicrobial agent to protect crops from bacterial infections, thereby increasing yield and reducing the need for chemical pesticides.
Used in Cosmetics Industry:
Due to its antimicrobial properties, 3-Quinolinecarboxylic acid can be employed in the cosmetics industry as a preservative to extend the shelf life of products and maintain their safety and efficacy.
Check Digit Verification of cas no
The CAS Registry Mumber 6480-68-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,8 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6480-68:
(6*6)+(5*4)+(4*8)+(3*0)+(2*6)+(1*8)=108
108 % 10 = 8
So 6480-68-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H7NO2/c12-10(13)8-5-7-3-1-2-4-9(7)11-6-8/h1-6H,(H,12,13)/p-1
6480-68-8Relevant articles and documents
Convenient synthesis of 3-Hydroxyquinolines via dakin oxidation: A short synthesis of Jineol
Ghorai, Sujit K.,Dasgupta, Mayukh,Dutta, Piyali,Dumeunier, Raphael,Mal, Sanjib,Patre, Rupesh,Kuilya, Tapan Kumar,Pal, Sitaram,Manjunath, Bhanu N.
supporting information, (2020/08/06)
A convenient synthesis of 3-hydroxyquinolines has been described via unprecedented Dakin oxidation of quinoline-3-carboxaldehydes. Subsequently, application of the methodology to a high yielding synthesis of quinoline alkaloid Jineol (1) is reported.
NMR studies of new heterocycles tethered to purine moieties with anticancer activity
Fernández-Sáez, Nerea,Campos, Joaquín M.,Camacho, María Encarnación,Carrión, María Dora
, p. 331 - 341 (2019/04/30)
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Tandem one-pot CO2 reduction by PMHS and silyloxycarbonylation of aryl/vinyl halides to access carboxylic acids
Paridala, Kumaraswamy,Lu, Sheng-Mei,Wang, Meng-Meng,Li, Can
supporting information, p. 11574 - 11577 (2018/10/31)
The present study discloses the synthesis of aryl/vinyl carboxylic acids from Csp2-bound halides (Cl, Br, I) in a carbonylative path by using silyl formate (from CO2 and hydrosilane) as an instant CO-surrogate. Hydrosilane provides hydride for reduction and its oxidation product silanol serves as a coupling partner. Mono-, di-, and tri-carboxylic acids were obtained from the corresponding aryl/vinyl halides.