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Sku CI27337_250_G
Chem Impex
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Product Information

Product Name
4-Chloropyridine hydrochloride
Brand Name
Chem Impex
Product Number
27337
CAS
7379-35-3
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
81852
IUPAC Name
4-chloropyridine;hydrochloride
InChI Key
XGAFCCUNHIMIRV-UHFFFAOYSA-N
SMILES
C1=CN=CC=C1Cl.Cl

Application

4-Chloropyridine hydrochloride is widely utilized in research focused on:

Synthesis of Pharmaceuticals: This compound serves as a key intermediate in the production of various pharmaceuticals, particularly in the synthesis of antiviral and anti-inflammatory drugs, enhancing their efficacy and reducing side effects.

Agricultural Chemicals: It is used in the formulation of agrochemicals, including herbicides and pesticides, contributing to improved crop yields and pest management strategies.

Laboratory Reagent: As a versatile reagent, it is employed in organic synthesis and analytical chemistry, aiding researchers in developing new compounds and conducting various chemical reactions.

Material Science: The compound is utilized in the development of specialty polymers and coatings, providing enhanced properties such as durability and resistance to environmental factors.

Research in Biochemistry: It plays a role in studying enzyme inhibitors and receptor interactions, offering insights into biological processes and potential therapeutic targets.

References

Anti-Markovnikov hydrochlorination and hydronitrooxylation of α-olefins via visible-light photocatalysis

Publication Name: Nature Catalysis
Publication Date: 2023-02-13
DOI: 10.1038/s41929-023-00914-7

4-Dimethylaminopyridine grafted on MCM-41 as an efficient and highly stable catalyst for the production of α-tocopherol acetate

Publication Name: Journal of Porous Materials
Publication Date: 2020-07-17
DOI: 10.1007/s10934-020-00939-4

Octenidine

Publication Name: Pharmaceutical Substances
Publication Date: 2018

Nano Sulfated Titania as a Heterogeneous Solid Acid Catalyst for the Synthesis of Pyrroles by Clauson–Kaas Condensation under Solvent-free Conditions

Publication Name: Chemistry of Heterocyclic Compounds
Publication Date: 2014-02-27
DOI: 10.1007/s10593-014-1425-3

Use of the Graebe-Ullmann reaction in the synthesis of 8-methyl-γ-carboline and isomeric aromatic aza-γ-carbolines

Publication Name: Chemistry of Heterocyclic Compounds
Publication Date: 2012-11-08
DOI: 10.1007/s10593-012-1127-7