320-38-7 Usage
Uses
Used in Pharmaceutical Synthesis:
4-Nitro-3-(trifluoromethyl)benzoic acid is utilized as an intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with improved therapeutic properties.
Used in Agricultural Chemical Synthesis:
4-NITRO-3-(TRIFLUOROMETHYL)BENZOIC ACID& is also employed in the production of agricultural chemicals, contributing to the development of more effective and safer agrochemicals for crop protection and pest control.
Used in Medicinal Chemistry Research:
4-Nitro-3-(trifluoromethyl)benzoic acid is used as a research molecule in medicinal chemistry, where its potential anti-inflammatory and anti-cancer properties are being investigated. The presence of the nitro and trifluoromethyl groups in its structure may contribute to its biological activity, making it a promising candidate for the development of new therapeutic agents.
Used in Chemical Synthesis Industry:
In the chemical synthesis industry, 4-nitro-3-(trifluoromethyl)benzoic acid serves as a key building block for the creation of various chemical compounds with diverse applications, including specialty chemicals and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 320-38-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,2 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 320-38:
(5*3)+(4*2)+(3*0)+(2*3)+(1*8)=37
37 % 10 = 7
So 320-38-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H4F3NO4/c9-8(10,11)5-3-4(7(13)14)1-2-6(5)12(15)16/h1-3H,(H,13,14)
320-38-7Relevant academic research and scientific papers
Physical gelation of polar aprotic solvents induced by hydrogen bonding modulation of polymeric molecules
Ka, Duyoun,Seo, Myungeun,Choi, Hyungsam,Kim, Eun Hee,Kim, Sang Youl
supporting information; scheme or table, p. 5722 - 5724 (2010/09/18)
Poly(aryl ether amide) containing o-nitroanilide forms a physical gel in polar aprotic solvents by solvent-induced change of hydrogen bonding modes, in which hydrogen bonding acceptor solvent molecules break intramolecular hydrogen bonding of o-nitroanili
Optimization of novel combi-molecules: Identification of balanced and mixed bcr-abl/DNA targeting properties
Rachid, Zakaria,Katsoulas, Athanasia,Williams, Christopher,Larroque, Anne-Laure,McNamee, James,Jean-Claude, Bertrand J.
, p. 4248 - 4253 (2008/02/09)
Steps toward the identification of combi-molecules with strong abl tyrosine kinase (TK) inhibitory property and significant DNA damaging potential are described. The optimized combi-molecule 13a was shown to induce approximately twofold stronger abl TK in
