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AI13940

1214365-08-8 | 2-(3-Fluorophenyl)nicotinic acid

Packsize Purity Availability Price Discounted Price    Quantity
1mg 2 weeks $105.00 $73.00 -   +
2mg 2 weeks $123.00 $86.00 -   +
3mg 2 weeks $149.00 $105.00 -   +
5mg 2 weeks $168.00 $118.00 -   +
10mg 2 weeks $193.00 $135.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AI13940
Chemical Name: 2-(3-Fluorophenyl)nicotinic acid
CAS Number: 1214365-08-8
Molecular Formula: C12H8FNO2
Molecular Weight: 217.19582320000004
MDL Number: MFCD00429496
SMILES: Fc1cccc(c1)c1ncccc1C(=O)O

 

Computed Properties
Complexity: 259  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 16  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 2  
XLogP3: 2.1  

 

 

Upstream Synthesis Route
  • The 2-(3-fluorophenyl)nicotinic acid is a versatile chemical compound commonly used in chemical synthesis procedures. This compound plays a crucial role in the field of organic chemistry due to its unique structural properties and reactivity.In chemical synthesis, 2-(3-fluorophenyl)nicotinic acid serves as a valuable building block for the preparation of various organic molecules. Its functional groups and aromatic ring structure make it an ideal precursor for the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. The fluorine substituent on the phenyl ring imparts specific properties to the compound, allowing for precise modifications and selective reactions during synthetic processes.This compound can be utilized in the creation of novel drug candidates, as well as intermediates for complex natural product synthesis. Its compatibility with a wide range of chemical reactions makes it a valuable tool for organic chemists seeking to design and produce new molecules with specific properties and functions. Whether used as a starting material or as a key intermediate, 2-(3-fluorophenyl)nicotinic acid offers versatility and potential for innovation in chemical synthesis endeavors.
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