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AH13162

6921-22-8 | 1,2-Difluoro-3-nitrobenzene

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $10.00 $7.00 -   +
1g 98% in stock $13.00 $9.00 -   +
5g 98% in stock $31.00 $22.00 -   +
10g 98% in stock $60.00 $42.00 -   +
25g 98% in stock $149.00 $105.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AH13162
Chemical Name: 1,2-Difluoro-3-nitrobenzene
CAS Number: 6921-22-8
Molecular Formula: C6H3F2NO2
Molecular Weight: 159.0903
MDL Number: MFCD00456802
SMILES: O=N(=O)c1cccc(c1F)F

 

Computed Properties
Complexity: 159  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 11  
Hydrogen Bond Acceptor Count: 4  
XLogP3: 1.8  

 

 

Upstream Synthesis Route
  • 2,3-Difluoronitrobenzene is a versatile chemical compound that finds wide applications in chemical synthesis. This compound is commonly used as a building block in the production of various pharmaceuticals, agrochemicals, and functional materials due to its unique chemical reactivity.In chemical synthesis, 2,3-Difluoronitrobenzene serves as a key intermediate for the introduction of fluorine atoms into organic molecules. The presence of the nitro and fluoro groups in its molecular structure allows for diverse transformation reactions, enabling the creation of complex organic compounds. Additionally, the fluorine atoms present in 2,3-Difluoronitrobenzene contribute to the stability and lipophilicity of the final products, enhancing their pharmacological properties and biological activities.Furthermore, 2,3-Difluoronitrobenzene is utilized in the synthesis of fluorinated building blocks, which are crucial for the development of novel materials with desirable properties such as high thermal stability, chemical resistance, and electron-withdrawing capabilities. Its ability to act as a fluorinated synthon makes it a valuable tool for the preparation of fluorinated polymers, dyes, and functionalized organic molecules in the field of materials science.Overall, the strategic incorporation of 2,3-Difluoronitrobenzene into synthetic pathways enables chemists to access a diverse array of fluorine-containing compounds with tailored properties, paving the way for the advancement of various industries including pharmaceuticals, agrochemicals, and materials science.
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