AA00693
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 95% | in stock | $12.00 | $9.00 | - + | |
1g | 95% | in stock | $23.00 | $17.00 | - + | |
5g | 95% | in stock | $32.00 | $23.00 | - + | |
10g | 95% | in stock | $63.00 | $45.00 | - + | |
25g | 95% | in stock | $156.00 | $110.00 | - + | |
100g | 95% | in stock | $600.00 | $420.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA00693 |
Chemical Name: | 2-(2-Chloro-3-fluorophenyl)acetic acid |
CAS Number: | 1000523-07-8 |
Molecular Formula: | C8H6ClFO2 |
Molecular Weight: | 188.5834432 |
MDL Number: | MFCD09925136 |
SMILES: | OC(=O)Cc1cccc(c1Cl)F |
Complexity: | 174 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 12 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 1 |
Rotatable Bond Count: | 2 |
XLogP3: | 2.1 |
2-(2-Chloro-3-fluorophenyl)acetic acid, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound plays a crucial role as a key intermediate in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique chemical structure allows for diverse functionalization and modification, making it a valuable building block in organic synthesis.In chemical synthesis, 2-(2-Chloro-3-fluorophenyl)acetic acid serves as a vital precursor for the synthesis of numerous biologically active compounds. It can be utilized to introduce the 2-(2-chloro-3-fluorophenyl)acetyl group into molecules, enabling the creation of new compounds with specific pharmacological or biological properties. Additionally, this compound is often employed as a starting material for the preparation of complex molecules through various synthetic routes.Furthermore, the functional groups present in 2-(2-Chloro-3-fluorophenyl)acetic acid facilitate its reactivity and compatibility with a wide range of chemical transformations. It can undergo processes such as esterification, amidation, and reduction to yield structurally diverse derivatives with tailored properties. This versatility makes it an indispensable tool for synthetic chemists seeking to develop novel compounds with potential applications in drug discovery, materials science, and other fields.