169507-61-3 Usage
Uses
Used in Pharmaceutical Industry:
2,4,5-TRIFLUORO-3-ETHOXY BENZOIC ACID is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to impart specific properties to the final drug molecules, enhancing their efficacy and pharmacokinetics.
Used in Agrochemical Industry:
In the agrochemical sector, 2,4,5-TRIFLUORO-3-ETHOXY BENZOIC ACID is utilized as a precursor in the development of agrochemicals, contributing to the creation of compounds with targeted pesticidal or herbicidal activities.
Used in Organic Synthesis:
2,4,5-TRIFLUORO-3-ETHOXY BENZOIC ACID is employed as a building block in organic synthesis, allowing for the construction of a wide range of specialty chemicals with diverse applications across various industries.
Used in Research and Development:
2,4,5-TRIFLUORO-3-ETHOXY BENZOIC ACID is also used in research and development settings to explore its potential biological and pharmacological activities, with the aim of discovering new therapeutic agents or gaining insights into molecular mechanisms.
Check Digit Verification of cas no
The CAS Registry Mumber 169507-61-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,5,0 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 169507-61:
(8*1)+(7*6)+(6*9)+(5*5)+(4*0)+(3*7)+(2*6)+(1*1)=163
163 % 10 = 3
So 169507-61-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H7F3O3/c1-2-15-8-6(11)4(9(13)14)3-5(10)7(8)12/h3H,2H2,1H3,(H,13,14)
169507-61-3Relevant academic research and scientific papers
The Synthesis, Structure-Activity, and Structure-Side Effect Relationships of a Series of 8-Alkoxy- and 5-Amino-8-alkoxyquinolone Antibacterial Agents
Sanchez, Joseph P.,Gogliotti, Rocco D.,Domagala, John M.,Gracheck, Stephen J.,Huband, Michael D.,et al.
, p. 4478 - 4487 (2007/10/03)
A series of 1-cyclopropyl-6-fluoro-8-alkoxy (8-methoxy and 8-ethoxy)-quinoline-3-carboxylic acids and 1-cyclopropyl-5-amino-6-fluoro-8-alkoxyquinoline-3-carboxylic acids has been prepared and evaluated for antibacterial activity.In addition, they were also compared to quinolones with classic substitution at C8 (H, F, Cl) and the naphthyridine nucleus in a phototoxicity and mammalian cell cytotoxiciry assay.The series of 8-methoxyquinolones had antibacterial activity against Gram-positive, Gram-negative, and anaerobic bacteria equivalent to that most active 8-substituted compounds (8-F and 8-Cl).There was also a concomitant reduction in several of the potential side effects (i.e., phototoxicity and clonogenicity) compared to the most active quinolones with classic substitution at C-8.The 8-ethoxy derivatives had an even better safety profile but were significantly less active (2-3 dilutions) in the antibacterial assay.
