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Sku CI33403_25_G
Chem Impex
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Product Information

Product Name
2-Chloro-5-nitropyridine-3-carbonitrile
Brand Name
Chem Impex
Product Number
33403
CAS
31309-08-7
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
586450
IUPAC Name
2-chloro-5-nitropyridine-3-carbonitrile
InChI Key
CSDMFMSXIUTEFJ-UHFFFAOYSA-N
SMILES
C1=C(C=NC(=C1C#N)Cl)N+(=O)O-

Application

2-Chloro-5-nitropyridine-3-carbonitrile is widely utilized in research focused on:

Pharmaceutical Development: This compound serves as an intermediate in the synthesis of various pharmaceuticals, particularly those targeting bacterial infections and cancer. Its unique structure allows for the development of novel drug candidates.

Agricultural Chemicals: It is used in the formulation of agrochemicals, including pesticides and herbicides, providing effective solutions for crop protection while minimizing environmental impact.

Material Science: The compound is explored in the creation of advanced materials, such as polymers and coatings, that require specific chemical properties for enhanced durability and performance.

Biochemical Research: Researchers utilize it in studies related to enzyme inhibition and receptor binding, contributing to a deeper understanding of biochemical pathways and potential therapeutic targets.

Analytical Chemistry: It serves as a reference standard in analytical methods, aiding in the detection and quantification of related compounds in various samples, ensuring accuracy in research and quality control.

References

Nitric oxide induces the distinct invisibility phenotype of Mycobacterium tuberculosis

Publication Name: Communications Biology
Publication Date: 2024-09-28
DOI: 10.1038/s42003-024-06912-0

Reactivity of 2-aminopyridine N-oxides

Publication Name: Russian Chemical Bulletin
Publication Date: 2024-01
DOI: 10.1007/s11172-024-4120-2

Synthesis and antileprosy activity of some dialkyldithiocarbamates

Publication Name: The Journal of antimicrobial chemotherapy
Publication Date: 2006-04-04
DOI: 10.1093/jac/dkl095

N-Arylation with Electrophilic Aryl or Hetaryl Groups

Publication Name: Science of Synthesis
Publication Date: 2005

Condensation of 2-Halonicotinates with Ureas and Amidines

Publication Name: Science of Synthesis
Publication Date: 2004