40335-02-2 Usage
Uses
Used in Pharmaceutical Industry:
2,3,4-trichloroquinoline is used as a building block for the synthesis of pharmaceuticals, as its chemical structure can be modified to create new drug candidates. 2,3,4-trichloroquinoline's versatility in chemical reactions allows for the development of novel therapeutic agents with potential applications in various medical fields.
Used in Agrochemical Industry:
2,3,4-trichloroquinoline is used as a building block for the synthesis of agrochemicals, such as pesticides and herbicides. Its chemical properties make it a valuable component in the development of new compounds that can effectively control pests and weeds in agricultural settings.
Used in Material Science:
2,3,4-trichloroquinoline is used in the development of new materials, as its unique chemical structure can contribute to the creation of novel materials with specific properties. This can include materials with enhanced stability, conductivity, or other desirable characteristics for various applications.
Used as an Antimicrobial Agent:
2,3,4-trichloroquinoline is used as an antimicrobial agent, demonstrating activity against various microorganisms. Its ability to inhibit the growth of bacteria and fungi makes it a potential candidate for use in disinfectants, sanitizers, and other products designed to maintain cleanliness and prevent the spread of infections.
Used as an Antifungal Agent:
2,3,4-trichloroquinoline is used as an antifungal agent, showing effectiveness against various fungal species. This property can be harnessed in the development of antifungal treatments for medical or agricultural use, helping to combat fungal infections and protect crops from fungal diseases.
Used in Organic Synthesis:
2,3,4-trichloroquinoline is used as a reagent in organic synthesis, where it can serve as a starting material or intermediate in the production of other organic compounds. Its reactivity and functional groups make it a valuable component in the synthesis of a wide range of chemical products, from pharmaceuticals to specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 40335-02-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,3,3 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 40335-02:
(7*4)+(6*0)+(5*3)+(4*3)+(3*5)+(2*0)+(1*2)=72
72 % 10 = 2
So 40335-02-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H4Cl3N/c10-7-5-3-1-2-4-6(5)13-9(12)8(7)11/h1-4H
40335-02-2Relevant academic research and scientific papers
Regioselective Azidation of 2,4-Dichloroquinolines
Steinschifter, Waltraud,Stadlbauer, Wolfgang
, p. 311 - 318 (2007/10/02)
Reactions of 2,4-dichloroquinolines (2a-f) with sodium azide in DMF lead either regioselectively to 4-azido-2-chloroquinolines (3a-f) or with excess of sodium azide and catalysts to 5-azido-tetrazoloquinolines (4a-f). 2,4-Dichloroquinolines (2g-i) having electron donating substituents in 3-position react with sodium azide in DMF to a mixture of 4-azido-2-chloroquinolines (3g-i) and 5-chlorotetrazoloquinolines (5g-i).When the reaction of the 2,4-dichloroquinolines (2a-i) with sodium azide is carried out in ethanol with addition of methanesulfonic acid, regioselectively 5-chloro-tetrazoloquinolines (5a-i) are obtained.Structural assignments of 3 and 5 have been carried out by 13C-NMR spectra, IR spectra and degradation reactions of the azido- and tetrazolo group to aminoquinolines (7 and 10) via iminophosphoranes (8 and 9).It could be shown that in 2-azido/tetrazolo-quinolines (4 and 5) the tetrazole ring structure is the dominant species.
2,4-Dihalogenoquinolines. Synthesis, Orientation Effects and 1H and 13C NMR Spectral Studies
Osborne, Alan G.,Buley, Jill M.,Clarke, Helen,Dakin, Rachel C. H.,Price, Paul I.
, p. 2747 - 2756 (2007/10/02)
Isomer ratios for the syntheses of 2,4-dichloroquinolines from meta-substituted and 3,4-disubstituted anilines are reported, a synthesis of 2,4-dibromoquinoline 1b is also described.The structures of certain bromination products 17 and 1f obtained from 4-hydroxy-2-quinolone have been revised.A thorough study of the 1H and 13C NMR spectra of a series of 2,4-dihalogenoquinolines is presented and the effects of the halogen substituents on JCH couplings are highlighted.
