AE19575
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
100mg | 98% | in stock | $57.00 | $40.00 | - + | |
250mg | 98% | in stock | $80.00 | $56.00 | - + | |
1g | 98% | in stock | $140.00 | $98.00 | - + | |
5g | 98% | in stock | $420.00 | $294.00 | - + | |
10g | 98% | in stock | $680.00 | $476.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AE19575 |
Chemical Name: | 5-Methoxypicolinimidamide hydrochloride |
CAS Number: | 1179359-60-4 |
Molecular Formula: | C7H10ClN3O |
Molecular Weight: | 187.6268 |
MDL Number: | MFCD12755551 |
SMILES: | COc1ccc(nc1)C(=N)N.Cl |
Complexity: | 149 |
Covalently-Bonded Unit Count: | 2 |
Heavy Atom Count: | 12 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 3 |
Rotatable Bond Count: | 2 |
5-Methoxypicolinimidamide hydrochloride is a versatile compound that finds application in various chemical synthesis processes. With its unique structure and properties, this compound serves as a valuable building block in the creation of novel organic molecules and pharmaceuticals. In chemical synthesis, 5-Methoxypicolinimidamide hydrochloride is utilized as an intermediate or reagent in the production of complex organic compounds. Its presence can facilitate the formation of key bonds or functional groups, enabling the efficient construction of target molecules. This compound's reactivity and compatibility with different reaction conditions make it a useful tool for organic chemists seeking to streamline their synthetic processes.Moreover, the incorporation of 5-Methoxypicolinimidamide hydrochloride into synthesis routes can impart specific properties or functions to the final products. Whether it acts as a protecting group, a nucleophile, or a precursor for further transformations, this compound's versatility opens up a range of possibilities for chemical synthesis practitioners. By leveraging its unique chemical characteristics, researchers can access new pathways and strategies for achieving their synthetic targets.