AE61958
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.
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 |
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 |
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.