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Home  > Chemistry  > Heterocyclic Building Blocks  > Pyridines  > 2,4,6-Trichloro-3-nitropyridine

AB52397

60186-13-2 | 2,4,6-Trichloro-3-nitropyridine

Packsize Purity Availability Price Discounted Price    Quantity
1g 98% in stock $43.00 $31.00 -   +
25g 98% in stock $914.00 $640.00 -   +
100g 98% in stock $3,370.00 $2,359.00 -   +

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*All prices are in USD.

Description
Catalog Number: AB52397
Chemical Name: 2,4,6-Trichloro-3-nitropyridine
CAS Number: 60186-13-2
Molecular Formula: C5HCl3N2O2
Molecular Weight: 227.4326
MDL Number: MFCD09264535
SMILES: Clc1cc(Cl)c(c(n1)Cl)[N+](=O)[O-]

 

Computed Properties
Complexity: 186  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 3  
XLogP3: 3.2  

 

 

Upstream Synthesis Route
  • 2,4,6-Trichloro-3-nitropyridine is a versatile compound commonly employed in chemical synthesis as a key building block. Its unique structure and reactive properties make it an important intermediate in the production of various pharmaceuticals, agrochemicals, and advanced materials.In organic synthesis, 2,4,6-Trichloro-3-nitropyridine serves as a valuable precursor for the synthesis of complex molecules. Its trichloro and nitro functional groups provide multiple sites for further derivatization, allowing chemists to introduce specific functionalities and modify the compound according to desired properties. Additionally, its pyridine ring imparts specific reactivity that can be harnessed in various transformations.One common application of 2,4,6-Trichloro-3-nitropyridine is in the synthesis of heterocyclic compounds, where its nitro group can undergo reduction or substitution reactions to introduce nitrogen-containing motifs into the final product. This compound is also utilized in the development of herbicides, insecticides, and fungicides due to its ability to confer desired biological activities to the target molecules.Furthermore, 2,4,6-Trichloro-3-nitropyridine finds utility in material science for the preparation of functionalized polymers, dyes, and catalysts. Its versatile nature and compatibility with various synthetic methodologies make it a valuable tool for chemists working in diverse fields of research and development.
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