AE19685
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 97% | in stock | $251.00 | $176.00 | - + | |
1g | 97% | in stock | $558.00 | $391.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AE19685 |
Chemical Name: | Isoquinoline-3-carboximidamide hydrochloride |
CAS Number: | 1179362-42-5 |
Molecular Formula: | C10H10ClN3 |
Molecular Weight: | 207.6595 |
MDL Number: | MFCD12755569 |
SMILES: | NC(=N)c1ncc2c(c1)cccc2.Cl |
Complexity: | 202 |
Covalently-Bonded Unit Count: | 2 |
Heavy Atom Count: | 14 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 3 |
Rotatable Bond Count: | 1 |
Isoquinoline-3-carboximidamide hydrochloride is a versatile chemical compound that finds application in chemical synthesis. This compound serves as a key building block in organic chemistry reactions, particularly in the formation of various heterocyclic compounds. Its unique structure and reactivity make it a valuable reagent for the creation of complex molecules with potential biological activity.In chemical synthesis, Isoquinoline-3-carboximidamide hydrochloride can be used as a precursor in the synthesis of pharmaceuticals, agrochemicals, and materials science. Its functional groups allow for selective derivatization, enabling chemists to tailor the molecule for specific applications. Through various synthetic transformations such as cyclization, oxidation, and reduction, this compound can be modified to introduce different substituents and functional groups, influencing the properties of the final products.Additionally, Isoquinoline-3-carboximidamide hydrochloride can participate in key reactions like cross-coupling, nucleophilic addition, and condensation, expanding its utility in the synthesis of diverse molecular structures. Its role in chemical synthesis extends to the development of new methodologies and strategies for efficient and selective bond formation, contributing to the advancement of synthetic organic chemistry.