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AA13392

114076-35-6 | 3,4-Difluoro-2-methoxyaniline

Packsize Purity Availability Price Discounted Price    Quantity
250mg 95% in stock $79.00 $55.00 -   +
1g 95% in stock $116.00 $81.00 -   +
5g 95% in stock $418.00 $292.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA13392
Chemical Name: 3,4-Difluoro-2-methoxyaniline
CAS Number: 114076-35-6
Molecular Formula: C7H7F2NO
Molecular Weight: 159.1333864
MDL Number: MFCD07368889
SMILES: COc1c(N)ccc(c1F)F

 

Computed Properties
Complexity: 134  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 11  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 1  
XLogP3: 1.4  

 

 

Upstream Synthesis Route
  • 3,4-Difluoro-2-methoxyaniline is a versatile chemical compound widely used in organic synthesis for its unique properties. This compound serves as a valuable building block in the development of various chemical processes and the synthesis of new molecules. In chemical synthesis, 3,4-Difluoro-2-methoxyaniline can act as a key intermediate in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. Its specific structural features make it an important reagent for introducing fluorine and methoxy functional groups into organic molecules, which can significantly enhance the properties and biological activities of the resulting compounds. Additionally, 3,4-Difluoro-2-methoxyaniline is often utilized in the preparation of dyes, pigments, and organic materials due to its ability to impart color and other desirable qualities. Its compatibility with a wide range of reaction conditions and its stability under various synthetic protocols make it a valuable tool for chemists working in diverse research areas. Overall, the application of 3,4-Difluoro-2-methoxyaniline in chemical synthesis offers exciting opportunities for creating novel compounds with tailored properties and functionalities, driving innovation in the field of organic chemistry.
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