1044209-44-0

Basic information

• Product Name: 3-CHLORO-4-(PYRIDIN-2-YL)ANILINE
• Synonyms: 3-CHLORO-4-(PYRIDIN-2-YL)ANILINE;3-chloro-4-(2-pyridinyl)Benzenamine
• CAS NO: 1044209-44-0
• Molecular Formula: C₁₁H₉ClN₂
• Molecular Weight: 204.65556
• Mol File: 1044209-44-0.mol

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 3-CHLORO-4-(PYRIDIN-2-YL)ANILINE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-CHLORO-4-(PYRIDIN-2-YL)ANILINE(1044209-44-0)
• EPA Substance Registry System: 3-CHLORO-4-(PYRIDIN-2-YL)ANILINE(1044209-44-0)

Safety Data

• Hazardous Substances Data: 1044209-44-0(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
3-Chloro-4-(pyridin-2-yl)aniline is used as a precursor 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 compounds with potential medicinal properties.
Used in Agrochemical Industry:
In the agrochemical sector, 3-chloro-4-(pyridin-2-yl)aniline is employed as a precursor for the synthesis of agrochemicals, such as pesticides and herbicides. Its incorporation into these products can enhance their effectiveness in controlling pests and weeds, thereby improving crop yields and quality.
Used in Dyes and Pigments Production:
3-Chloro-4-(pyridin-2-yl)aniline is utilized as an intermediate in the production of dyes and pigments, imparting color to various materials and products. Its chemical properties enable the creation of stable and vibrant colorants for use in industries such as textiles, plastics, and paints.
Safety Precautions:
Given its hazardous nature, 3-chloro-4-(pyridin-2-yl)aniline should be handled and stored with caution. Proper safety measures, including the use of personal protective equipment and adherence to safety guidelines, are essential to minimize risks associated with its use.

Upstream product

• 4381-32-2 2-(2-chlorophenyl)pyridine 
• 4420-82-0 2-(2-chloro-4-nitrophenyl)pyridine 

Downstream Products

• 1044209-45-1 C₂₁H₂₂ClN₃O₂ 

Relevant articles and documents

Divergent Late-Stage (Hetero)aryl C?H Amination by the Pyridinium Radical Cation

(Hetero)arylamines constitute some of the most prevalent functional molecules, especially as pharmaceuticals. However, structurally complex aromatics currently cannot be converted into arylamines, so instead, each product isomer must be assembled through a multistep synthesis from simpler building blocks. Herein, we describe a late-stage aryl C?H amination reaction for the synthesis of complex primary arylamines that other reactions cannot access directly. We show and rationalize through a mechanistic analysis the reasons for the wide substrate scope and the constitutional diversity of the reaction, which gives access to molecules that would not have been readily available otherwise.

Theramutein modulators

This invention relates to agents that are inhibitors or activators of variant forms of endogenous proteins and novel methods of identifying such variants. Of particular interest are inhibitors and activators of endogenous protein variants, encoded by genes which have mutated, which variants often arise or are at least first identified as having arisen following exposure to a chemical agent which is known to be an inhibitor or activator of the corresponding unmutated endogenous protein.

THERAMUTEIN MODULATORS

This invention relates to agents that are inhibitors or activators of variant forms of endogenous proteins and novel methods of identifying such variants. Of particular interest are inhibitors and activators of endogenous protein variants, encoded by genes which have mutated, which variants often arise or are at least first identified as having arisen following exposure to a chemical agent which is known to be an inhibitor or activator of the corresponding unmutated endogenous protein.