402-17-5

Usage

Uses

Used in Pharmaceutical Industry:
2-Nitro-5-(trifluoromethyl)phenol is used as an intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique chemical structure allows for the creation of diverse medicinal compounds with potential health benefits.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Nitro-5-(trifluoromethyl)phenol serves as a raw material for the production of pesticides and other agricultural chemicals. Its properties enable the development of effective solutions for pest control and crop protection, enhancing agricultural productivity.
Used in Dye Industry:
2-Nitro-5-(trifluoromethyl)phenol is utilized as an intermediate in the manufacturing of dyes, imparting color to various materials and textiles. Its chemical properties facilitate the creation of stable and vibrant dyes for a wide range of applications.
Used in Organic Solvent Industry:
As a stabilizer in organic solvents, 2-Nitro-5-(trifluoromethyl)phenol helps maintain the stability and performance of these solvents in various industrial processes. Its presence enhances the longevity and effectiveness of solvents used in manufacturing and other applications.
Used in Fragrance Industry:
2-Nitro-5-(trifluoromethyl)phenol is employed as an intermediate in the production of fragrances and other aromatic chemicals. Its unique scent profile and chemical properties contribute to the creation of distinct and appealing fragrances for various consumer products.
Used in Antimicrobial Research:
2-Nitro-5-(trifluoromethyl)phenol has been studied for its potential antimicrobial properties, making it a candidate for further research in the development of new antimicrobial agents. Its ability to inhibit the growth of microorganisms could lead to innovative solutions in healthcare and other industries.
Used in Antioxidant Research:
2-NITRO-5-(TRIFLUOROMETHYL)PHENOL's potential antioxidant properties have also been investigated, with research exploring its capacity to neutralize harmful free radicals. This could pave the way for new applications in the field of antioxidants, offering protection against oxidative stress and related conditions.

InChI:InChI=1/C7H4F3NO3/c8-7(9,10)4-1-2-5(11(13)14)6(12)3-4/h1-3,12H

Upstream product

• 402-14-2 2-nitro-5-(trifluoromethyl)aniline 
• 402-54-0 p-nitrobenzotrifluoride 
• 402-11-9 3-chloro-4-nitrobenzotrifluoride 
• 98-17-9 3-Trifluoromethylphenol 

Downstream Products

• 907587-46-6 methyl 4-[(2-nitro-5-(trifluoromethyl)phenoxy)methyl]benzoate 
• 209688-18-6 2-nitro-5-trifluoromethylphenyl methoxymethyl ether 
• 914636-97-8 2-methoxy-1-nitro-4-(trifluoromethyl)benzene 
• 1413929-93-7 C₁₅H₁₁ClF₃NO₂S 
• 1413930-09-2 C₁₅H₉ClF₃NO₂ 
• 1413929-86-8 C₁₅H₁₁ClF₃NO₂S 
• 1413930-03-6 C₁₅H₉ClF₃NO₂ 
• 609850-66-0 C₂₃H₂₂F₇NO₂ 
• 343340-72-7 2-amino-5-trifluoromethyl-phenol hydrochloride 
• 442-79-5 4-nitro-benzoic acid-(6-trifluoromethyl-[8]quinolyl ester) 
• 391-49-1 toluene-4-sulfonic acid-(6-trifluoromethyl-[8]quinolyl ester) 
• 90800-42-3 8-hydroxy-quinoline-6-carboxylic acid 
• 321-70-0 6-trifluoromethyl-quinolin-8-ol 
• 209686-79-3 methyl 4-{[2-[(cyclopentylmethyl)(phenylsulfonyl)amino]-5-(trifluoromethyl)phenoxy]methyl}benzoate 

Relevant academic research and scientific papers

Vapochromic Luminescent π-Conjugated Systems with Reversible Coordination-Number Control of Hypervalent Tin(IV)-Fused Azobenzene Complexes

The dynamic and reversible changes of coordination numbers between five and six in solution and solid states, based on hypervalent tin(IV)-fused azobenzene (TAz) complexes, are reported. It was found that the TAz complexes showed deep-red emission owing t

HMOX1 inducers

The present invention is related to compounds of structure (I) as heme oxygenase 1 (HMOX 1) inducers. The present invention is also related a method of controlling the activity or the amount, or both the activity and the amount, of heme-oxygenase 1 in a mammalian subject. The definitions of the variables are provided herein.

Synthesis and in vitro antimycobacterial and isocitrate lyase inhibition properties of novel 2-methoxy-2′-hydroxybenzanilides, their thioxo analogues and benzoxazoles

A new series of 2-methoxy-2′-hydroxybenzanilide derivatives and their thioxo analogues have been synthesised and characterised by IR, NMR and elemental analysis. These compounds were investigated for their in vitro antimycobacterial activities against Mycobacterium tuberculosis 331/88, Mycobacterium avium 330/88, Mycobacterium kansasii 235/80, clinically isolated M. kansasii 6509/96 and the ability to act as in vitro isocitrate lyase inhibitors. The best ICL inhibitors were two compounds from the thiobenzanilide group (8f, 8m), which exhibited an inhibition potential that was equal to the standard compound, 3-nitropropionic acid. In addition, the best antimycobacterial properties were exhibited by benzanilide derivatives 6h, 6k and 6l with 5-Cl and 4′ or 5′ Cl/Br substitution. For all the thiobenzanilide derivatives tested, two conformers were observed in the NMR spectra, which is most likely due to the hindered rotation of the C-N bond.

COMPOSITION AND METHOD FOR CONTROLLING ARTHROPOD PESTS

The present invention provides: an arthropod pests control composition comprising, as active ingredients, a condensed heterocyclic compound and a pyrethroid compound; a method for controlling arthropod pests which comprises applying effective amounts of a condensed heterocyclic compound and a pyrethroid compound to the arthropod pests or a locus where the arthropod pests inhabit; and so on.

High-efficiency tris(8-hydroxyquinoline)aluminum (Alq3) complexes for organic white-light-emitting diodes and solid-state lighting

Combinations of electron-withdrawing and -donating substituents on the 8-hydroxyquinoline ligand of the tris(8-hydroxyquinoline)aluminum (Alq 3) complexes allow for control of the HOMO and LUMO energies and the HOMO-LUMO gap responsible for emission from the complexes. Here, we present a systematic study on tuning the emission and electroluminescence (EL) from Alq3 complexes from the green to blue region. In this study, we explored the combination of electron-donating substituents on C4 and C6. Compounds 1-6 displayed the emission tuning between 478 and 526 nm, and fluorescence quantum yield between 0.15 and 0.57. The compounds 2-6 were used as emitters and hosts in organic light-emitting diodes (OLEDs). The highest OLED external quantum efficiency (EQE) observed was 4.6 %, which is among the highest observed for Alq3 complexes. Also, the compounds 3-5 were used as hosts for red phosphorescent dopants to obtain white light-emitting diodes (WOLED). The WOLEDs displayed high efficiency (EQE up to 19 %) and high white color purity (color rendering index (CRI≈85). Whiter than white: Electron-withdrawing and -donating substituents on the tris(8-hydroxyquinoline) AlIII (Alq3) complexes allow for control of the emission and electroluminescence from green (526 nm) to the blue region (487 nm), and of the fluorescence quantum yield (0.15-0.57). The compounds used as emitters in OLEDs show a maximum external quantum efficiency (EQE) of 4.6 %, which is among the highest observed for Alq3 complexes. The complexes were used in white-light emitting OLEDs achieving high efficiency (EQE ≈19 %) and high white color purity (CRI≈85).

HARMFUL ARTHROPOD CONTROL COMPOSITION, AND FUSED HETEROCYCLIC COMPOUND

Disclosed is a harmful arthropod control composition comprising, as an active ingredient, a fused heterocyclic compound represented by formula (1) [wherein A1 and A2 independently represent a nitrogen atom or the like; R1 and R4 independently represent a halogen atom or the like; R2 and R3 independently represent a halogen atom or the like; R5 and R6 independently represent a linear C1-C6 hydrocarbon group which may be substituted, or the like (provided that both R5 and R6 cannot represent a hydrogen atom simultaneously); and n represents 0 or 1]. The harmful arthropod control composition has an excellent efficacy to control harmful arthropods.

HARMFUL ARTHROPOD CONTROL COMPOSITION, AND FUSED HETEROCYCLIC COMPOUND

Disclosed is a harmful arthropod control composition comprising, as an active ingredient, a fused heterocyclic compound represented by formula (1) [wherein A1 and A2 independently represent a nitrogen atom or the like; R1 and R4 independently represent a halogen atom or the like; R2 and R3 independently represent a halogen atom or the like; R5 and R6 independently represent a linear C1-C6 hydrocarbon group which may be substituted, or the like (provided that both R5 and R6 cannot represent a hydrogen atom simultaneously); and n represents 0 or 1]. The harmful arthropod control composition has an excellent efficacy to control harmful arthropods.

COMPOSITION AND METHOD FOR CONTROLLING ARTHROPOD PESTS

The present invention provides: an arthropod pests control composition comprising, as active ingredients, a condensed heterocyclic compound and a neonicotinoid compound; a method for controlling arthropod pests which comprises applying effective amounts of a condensed heterocyclic compound and a neonicotinoid compound to the arthropod pests or a locus where the arthropod pests inhabit; and so on.

COMPOSITION AND METHOD FOR CONTROLLING ARTHROPOD PESTS

The present invention provides: an arthropod pests control composition comprising, as active ingredients, a condensed heterocyclic compound and pyriproxyfen; a method for controlling arthropod pests which comprises applying effective amounts of a condensed heterocyclic compound and pyriproxyfen to the arthropod pests or a locus where the arthropod pests inhabit; and so on.

COMPOSITION AND METHOD FOR CONTROLLING ARTHROPOD PESTS

The present invention provides: an arthropod pests control composition comprising, as active ingredients, a condensed heterocyclic compound and pyridalyl; a method for controlling arthropod pests which comprises applying effective amounts of a condensed heterocyclic compound and pyridalyl to the arthropod pests or a locus where the arthropod pests inhabit; and so on.