2-Naphthalenecarboxamide, 3-amino- is an organic compound characterized by its naphthalene backbone, which consists of two fused aromatic rings. The presence of an amine group (-NH2) at the 3-position and a carboxamide group (-C(=O)NH2) at the 2-position contributes to its chemical properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of the amide functional group, which can engage in hydrogen bonding. It may also display various functional properties, including potential biological activity, making it of interest in pharmaceutical research. The compound's structure allows for potential interactions with biological targets, which can be explored in medicinal chemistry. Additionally, its stability and reactivity can be influenced by the electronic effects of the naphthalene system and the functional groups attached to it. Overall, 2-Naphthalenecarboxamide, 3-amino- is a compound of interest in both synthetic and applied chemistry contexts.

2-Naphthalenecarboxamide, 3-amino-

3-aMino-2-naphthaMide

3-Amino-2-naphthamide is a synthetic compound that has been used in the synthesis of quinazolinones and amines. This compound is a ligand for sildenafil, which is used as an anti-anginal drug. 3-Amino-2-naphthamide has been used to control the reaction conditions for cross coupling reactions with alkylating agents and organometallic compounds. The use of this compound can be applied to other methods, such as preparative methods, to increase their efficiency and productivity. This method has been shown to be more sustainable than other techniques.

CAS 27533-32-0: 2-Naphthalenecarboxamide, 3-amino-

3-aMino-2-naphthaMide

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3-Amino-2-naphthamide

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3-Amino-2-Naphthamide

Ref: 54-OR1026303

3-Amino-2-naphthamide

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