5324-31-2

Usage

Uses

Used in Pharmaceutical Industry:
2-[[[(2-FLUOROBENZOYL)AMINO]THIOXOMETHYL]AMINO]-3,5-DIIODO-BENZOIC ACID is used as a precursor or intermediate in the synthesis of other organic compounds for medicinal purposes. Its unique structure and the presence of fluorine and iodine atoms may contribute to its potential antimicrobial, antifungal, or antiviral properties, making it a valuable component in the development of new drugs and therapies.
Used in Research Applications:
2-[[[(2-FLUOROBENZOYL)AMINO]THIOXOMETHYL]AMINO]-3,5-DIIODO-BENZOIC ACID is used as a research compound to study its chemical properties and potential applications in various fields. Researchers may explore its interactions with biological systems, its ability to inhibit or modulate specific biological processes, and its potential as a therapeutic agent for various diseases and conditions.
Note: The specific uses and potential benefits of 2-[[[(2-FLUOROBENZOYL)AMINO]THIOXOMETHYL]AMINO]-3,5-DIIODO-BENZOIC ACID may vary depending on the research or application in which it is being used. Further studies and investigations are required to fully understand its capabilities and optimize its use in various industries.

Upstream product

• 109-65-9 1-bromo-butane 
• 92-87-5 p,p'-diaminobiphenyl 
• 71-36-3 butan-1-ol 

Relevant academic research and scientific papers

Compound, intermediate thereof, and application of compound in organic electroluminescent device

The invention relates to a compound, an intermediate thereof and an application of the compound in an organic electroluminescent device. The compound has a structure as shown in a formula I. The compound is applied to the organic electroluminescent device, and especially acts as a light extraction layer material, a phosphorescent host material, a hole injection layer material or a hole transport layer material to make the device have relatively high luminous efficiency and relatively low driving voltage.

Efficient nickel-catalysed: N -alkylation of amines with alcohols

The selective N-alkylation of amines with alcohols via the borrowing hydrogen strategy represents a prominent sustainable catalytic method, which produces water as the only by-product and is ideally suited for the catalytic transformation of widely available alcohol reaction partners that can be derived from renewable resources. Intensive research has been devoted to the development of novel catalysts that are mainly based on expensive noble metals. However, the availability of homogeneous or heterogeneous non-precious metal catalysts for this transformation is very limited. Herein we present a highly active and remarkably easy-to-prepare Ni based catalyst system for the selective N-alkylation of amines with alcohols, that is in situ generated from Ni(COD)2 and KOH under ligand-free conditions. This novel method is very efficient for the functionalization of aniline and derivatives with a wide range of aromatic and aliphatic alcohols as well as diols and exhibits excellent functional group tolerance including halides, benzodioxane and heteroaromatic groups. Several TEM measurements combined with elemental analysis were conducted in order to gain insight into the nature of the active catalyst and factors influencing reactivity.