790692-90-9

Usage

Uses

Used in Pharmaceutical Industry:
6-Chloro-5-iodo-3-nitropyridin-2-amine is utilized as a building block for the synthesis of a variety of biologically active molecules and pharmaceutical drugs. Its unique structure and properties contribute to the development of new therapeutic agents with potential applications in treating various diseases and conditions.
Used in Chemical Industry:
In the chemical industry, 6-Chloro-5-iodo-3-nitropyridin-2-amine serves as an important intermediate in the production of a wide range of chemical products. Its versatility and reactivity make it a key component in the synthesis of various compounds for different applications.
Used in Organic Chemistry Research and Development:
6-Chloro-5-iodo-3-nitropyridin-2-amine is also an important compound in the field of organic chemistry research and development. Its unique structure and properties provide opportunities for further exploration and innovation, leading to the discovery of new chemical reactions and the development of novel synthetic methods.

Upstream product

• 27048-04-0 2-amino-6-chloro-3-nitropyridine 

Downstream Products

• 1473416-56-6 6-chloro-5-(2,3-dichlorophenyl)pyridine-2,3-diamine 

Relevant academic research and scientific papers

Molecular recognition systems with pyrimidine analog pairing

This invention is for a new molecular recognition system, where DNA-like molecules comprising segments built from nucleotides that carry only a small which comprises process by which one molecule interacts with a specific second molecule, or by which a portion of a single molecule interacts specifically with another portion of the same molecule. Further, this invention relates to molecular recognition that follows simple rules. Further, this invention relates to molecular systems that are linear biopolymers that are analogs of DNA and RNA, in that they are built from a small set of building blocks that are linked together by phosphate groups, where the building blocks comprise a sugar (ribose, 2′-deoxyribose, or an analog) attached to a heterocycle. The molecular recognition that they display differs from that displayed by DNA and RNA, in that the rules governing molecular recognition break the rules of size complementarity followed in molecular recognition displayed between and within strands of DNA and RNA.

PARASITICIDAL COMPOSITIONS COMPRISING BENZIMIDAZOLE DERIVATIVES, METHODS AND USES THEREOF

The invention relates to oral, topical or injectable compositions for combating liver fluke parasites in mammals, comprising at least one benzimidazole derivative active agent. The invention also provides for an improved method for eradicating and controlling liver fluke parasite infections and infestations in a mammal comprising administering the compositions of the invention to the mammal in need thereof.

IMIDAZOPYRIDINE DERIVATIVES AS A2B ADENOSINE RECEPTOR ANTAGONISTS

New imidazopyrdidine derivatives of formula (I) are disclosed as antagonists of the A28 adenosine receptor.