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Sku CI30712_5_G
Chem Impex
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Product Information

Product Name
2,4,6-Trichloro-5-nitropyrimidine
Brand Name
Chem Impex
Product Number
30712
CAS
4359-87-9
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
4297843
IUPAC Name
2,4,6-trichloro-5-nitropyrimidine
InChI Key
QGFWFWSBFMRDNP-UHFFFAOYSA-N
SMILES
C1(=C(N=C(N=C1Cl)Cl)Cl)N+(=O)O-

Application

2,4,6-Trichloro-5-nitropyrimidine is widely utilized in research focused on:

Agricultural Chemicals: This compound serves as a key intermediate in the synthesis of herbicides, helping to control unwanted plant growth effectively.

Pharmaceutical Development: It is used in the synthesis of various pharmaceutical agents, particularly those targeting bacterial infections, enhancing the development of new medications.

Analytical Chemistry: The compound is employed as a reagent in analytical methods, aiding in the detection and quantification of other chemical substances in complex mixtures.

Material Science: It plays a role in the development of specialized materials, including polymers and coatings, which require specific chemical properties for enhanced performance.

Research Applications: This chemical is utilized in academic and industrial research settings to explore new chemical reactions and pathways, contributing to advancements in organic chemistry.

References Data Source From Pubchem

Synthesis of Biologically Active Seven-Membered-Ring Heterocycles

Publication Name: Synthesis
Publication Date: 2013-10-24
DOI: 10.1055/s-0033-1338549

Reactions of 4(6)-chloro-5-nitropyrimidines with nucleophilic agents (review)

Publication Name: Pharmaceutical Chemistry Journal
Publication Date: 1993-04
DOI: 10.1007/bf00810974

Pyrimidinetetrasulfonic acid

Publication Name: Chemistry of Heterocyclic Compounds
Publication Date: 1986-05
DOI: 10.1007/bf00519548

Sigma complexes in the pyrimidine series. 5. Reaction of 5-nitromethoxypyrimidines with the anion of malonic acid dinitrile

Publication Name: Chemistry of Heterocyclic Compounds
Publication Date: 1982-05
DOI: 10.1007/bf00526093