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Usage

Uses

Used in Pharmaceutical Synthesis:
(4-CHLORO-BENZYL)-PYRIDIN-3-YL-AMINE DIHYDROCHLORIDE is used as a reagent in the pharmaceutical industry for the synthesis of various pharmaceuticals and biologically active molecules. Its unique chemical structure allows for the development of new drugs with potential therapeutic benefits.
Used in Organic Synthesis:
In the field of organic chemistry, (4-CHLORO-BENZYL)-PYRIDIN-3-YL-AMINE DIHYDROCHLORIDE is used as a building block for the creation of complex organic compounds. Its versatile structure enables chemists to explore new pathways and synthesize novel molecules with potential applications in various industries.
Used in Drug Development:
(4-CHLORO-BENZYL)-PYRIDIN-3-YL-AMINE DIHYDROCHLORIDE is used as a key component in the development of new drugs for medical purposes. Its potential biological activities make it a valuable candidate for further research and development, with the aim of discovering new treatments for various diseases and conditions.
Used in Research and Development:
In the research and development sector, (4-CHLORO-BENZYL)-PYRIDIN-3-YL-AMINE DIHYDROCHLORIDE is employed as a test compound to study its interactions with other molecules and to understand its potential effects on biological systems. This information can be crucial in the development of new drugs and therapies.

Upstream product

• 104-88-1 4-chlorobenzaldehyde 
• 462-08-8 pyridin-3-ylamine 
• 873-76-7 para-Chlorobenzyl alcohol 

Relevant academic research and scientific papers

Green and scalable aldehyde-catalyzed transition metal-free dehydrative N-alkylation of amides and amines with alcohols

In contrast to the borrowing hydrogen-type N-alkylation reactions, in which alcohols were activated by transition metal-catalyzed anaerobic dehydrogenation, the addition of external aldehydes was accidentally found to be a simple and effective protocol for alcohol activation. This interesting finding subsequently led to an efficient and green, practical and scalable aldehyde-catalyzed transition metal-free dehydrative N-alkylation method for a variety of amides, amines, and alcohols. Mechanistic studies revealed that this reaction most possibly proceeds via a simple but interesting transition metal-free relay race mechanism. Copyright

Synthesis and microbiological evaluations of (N-heteroaryl)arylmethanamines and their Schiff bases

The synthesis as well as the antimicrobial and antiviral activities of new (N-heteroaryl)arylmethanamines and their Schiff bases are reported. None of the tested compounds showed activity against Herpes simplex virus type 2 and against Gram positive and Gram negative bacteria. Weak or moderate activity on poliovirus Sabin type 1, on reverse transcriptase and against Cryptococcus neoformans was shown by some of the tested compounds. Viceversa several synthesized compounds exhibited a moderate or good activity against strains of Candida albicans, while only some of the tested compounds were found moderately active against strains of Candida sp. Instead numerous new compounds 3 or 4 were active as control against isolates of plant pathogenic fungi. The obtained results are discussed on the basis of structure-activity relationships.

Fungicidal amines

N,N-Disubstituted heterocyclic amines are useful as fungicides.