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AB53657

1133122-96-9 | 2-Fluoro-4-hydroxybenzamide

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $17.00 $12.00 -   +
1g 98% in stock $67.00 $47.00 -   +
25g 98% in stock $1,535.00 $1,074.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB53657
Chemical Name: 2-Fluoro-4-hydroxybenzamide
CAS Number: 1133122-96-9
Molecular Formula: C7H6FNO2
Molecular Weight: 155.1264
MDL Number: MFCD09999525
SMILES: Oc1ccc(c(c1)F)C(=O)N

 

Computed Properties
Complexity: 163  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 11  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 1  
XLogP3: 0.9  

 

 

Upstream Synthesis Route
  • 2-Fluoro-4-hydroxybenzamide, also known as $name$, is a versatile compound widely utilized in chemical synthesis processes. With its unique structure and properties, $name$ plays a crucial role in various organic reactions and transformations.One of the key applications of 2-Fluoro-4-hydroxybenzamide in chemical synthesis is as a key intermediate in the preparation of pharmaceutical compounds. Its functional groups and reactivity make it a valuable building block in the synthesis of biologically active molecules. Additionally, $name$ can serve as a precursor in the creation of specialized chemicals used in research and industrial applications.In organic synthesis, 2-Fluoro-4-hydroxybenzamide can participate in a range of reactions such as acylation, amidation, and substitution reactions. Its fluoro and hydroxyl groups enable diverse functionalization possibilities, allowing for the generation of new compounds with tailored properties.Furthermore, the presence of the benzamide moiety in 2-Fluoro-4-hydroxybenzamide imparts stability and specific reactivity characteristics, making it a valuable component in the development of advanced synthetic routes.Overall, the versatility and reactivity of 2-Fluoro-4-hydroxybenzamide make it a valuable tool in chemical synthesis, contributing to the creation of innovative molecules with diverse applications.
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