AB04912
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
1g | 95% | in stock | $48.00 | $34.00 | - + | |
5g | 95% | in stock | $177.00 | $124.00 | - + | |
10g | 95% | in stock | $331.00 | $232.00 | - + | |
25g | 95% | in stock | $619.00 | $433.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB04912 |
Chemical Name: | 3-Chloro-6-phenylpyridazine |
CAS Number: | 20375-65-9 |
Molecular Formula: | C10H7ClN2 |
Molecular Weight: | 190.62897999999998 |
MDL Number: | MFCD00075253 |
SMILES: | Clc1ccc(nn1)c1ccccc1 |
NSC Number: | 28739 |
Complexity: | 157 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 13 |
Hydrogen Bond Acceptor Count: | 2 |
Rotatable Bond Count: | 1 |
XLogP3: | 2.5 |
3-Chloro-6-phenylpyridazine is a valuable building block in chemical synthesis, commonly used in the pharmaceutical and agrochemical industries. Its unique structure allows for versatile applications in the creation of various compounds with diverse properties. One key application of 3-Chloro-6-phenylpyridazine is in the synthesis of heterocyclic compounds, particularly in the formation of fused ring systems. The chloro group and phenyl ring on the pyridazine scaffold provide points for further derivatization, enabling the introduction of different functional groups to tailor the compound's properties for specific applications.Furthermore, 3-Chloro-6-phenylpyridazine serves as a precursor for the synthesis of biologically active molecules, including potential drug candidates and pesticides. Its ability to participate in various chemical reactions, such as Suzuki coupling, nucleophilic substitution, and metal-catalyzed processes, makes it a versatile intermediate in organic synthesis.Overall, 3-Chloro-6-phenylpyridazine plays a crucial role in the development of novel compounds with diverse applications in the fields of medicinal chemistry and agricultural chemistry. Its structural features and reactivity make it a valuable component in the toolbox of synthetic chemists seeking to design molecules with specific biological activities or agricultural properties.
Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501