CAS 5651-14-9
:naphthalene-2-carboximidamide
Description:
Naphthalene-2-carboximidamide, with the CAS number 5651-14-9, is an organic compound characterized by its naphthalene ring structure substituted with a carboximidamide functional group. This compound typically appears as a crystalline solid and is known for its aromatic properties due to the presence of the naphthalene moiety. Naphthalene-2-carboximidamide is soluble in polar organic solvents, which can facilitate its use in various chemical reactions and applications. The presence of the carboximidamide group imparts specific reactivity, making it a potential candidate for synthesis in medicinal chemistry and materials science. Additionally, this compound may exhibit biological activity, although specific pharmacological properties would require further investigation. Its stability and reactivity can be influenced by environmental factors such as pH and temperature, which are important considerations in its handling and application. Overall, naphthalene-2-carboximidamide represents a versatile compound with potential utility in various chemical and pharmaceutical contexts.
Formula:C11H10N2
InChI:InChI=1/C11H10N2/c12-11(13)10-6-5-8-3-1-2-4-9(8)7-10/h1-7H,(H3,12,13)
SMILES:c1ccc2cc(ccc2c1)C(=N)N
Synonyms:- 2-Naphthalenecarboximidamide
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Naphthalene-2-carboximidamide
CAS:<p>Naphthalene-2-carboximidamide is a benzamidine derivative that interacts with the active site of serine proteases. It was shown to have potent inhibitory potency against a number of proteinases, including urokinase-type plasminogen activator (uPA), matrix metalloproteinase-9 (MMP-9), and cathepsin G. The interaction of naphthalene-2-carboximidamide with uPA was specific and led to inhibition of its catalytic activity. Naphthalene-2-carboximidamide has been tested in clinical trials for the treatment of influenza.</p>Formula:C11H10N2Purity:Min. 95%Molecular weight:170.21 g/mol
