logo
Home  > Chemistry  > Heterocyclic Building Blocks  > Pyridines  > 2-Chloro-5-phenylisonicotinic acid

AE61958

1214323-23-5 | 2-Chloro-5-phenylisonicotinic acid

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $185.00 $130.00 -   +
250mg 95% in stock $355.00 $248.00 -   +
1g 95% in stock $766.00 $536.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AE61958
Chemical Name: 2-Chloro-5-phenylisonicotinic acid
CAS Number: 1214323-23-5
Molecular Formula: C12H8ClNO2
Molecular Weight: 233.6504
MDL Number: MFCD14701690
SMILES: Clc1ncc(c(c1)C(=O)O)c1ccccc1

 

Computed Properties
Complexity: 253  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 16  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 2  
XLogP3: 3  

 

 

Upstream Synthesis Route
  • 2-Chloro-5-phenylisonicotinic acid, also known as $name$, is a versatile chemical compound that finds significant application in organic synthesis. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals due to its unique chemical properties.In chemical synthesis, 2-Chloro-5-phenylisonicotinic acid acts as a valuable starting material for the preparation of heterocyclic compounds and complex organic molecules. Its chloro and phenyl functional groups enable it to participate in a variety of reactions, including nucleophilic substitutions, Friedel-Crafts acylations, and Suzuki-Miyaura cross-coupling reactions.Furthermore, the presence of the isonicotinic acid moiety in this compound enhances its reactivity towards metal catalysts, making it a useful ligand in transition metal-catalyzed reactions. This feature allows for the efficient construction of carbon-carbon and carbon-heteroatom bonds, facilitating the synthesis of structurally diverse compounds.Additionally, 2-Chloro-5-phenylisonicotinic acid can be modified through various derivatization reactions to introduce different functional groups, thereby expanding its utility in organic synthesis. Its versatility and compatibility with a wide range of reaction conditions make it a valuable tool for chemists working in medicinal chemistry, material science, and other related fields.
FEATURED PRODUCTS