2-Amino-4-methoxybenzaldehyde, with the CAS number 59236-36-1, is an organic compound characterized by its aromatic structure featuring both an amino group and a methoxy group attached to a benzaldehyde moiety. This compound typically appears as a solid or crystalline substance and is known for its pale yellow to off-white color. It has a molecular formula that reflects the presence of an amino group (-NH2), a methoxy group (-OCH3), and an aldehyde group (-CHO), contributing to its reactivity and potential applications in organic synthesis. The amino group can participate in various reactions, such as nucleophilic substitutions, while the aldehyde group can undergo oxidation or condensation reactions. 2-Amino-4-methoxybenzaldehyde is often used in the synthesis of pharmaceuticals, agrochemicals, and dyes, owing to its functional groups that allow for further chemical modifications. Additionally, it may exhibit biological activity, making it of interest in medicinal chemistry. Proper handling and storage are essential due to its potential reactivity and the need for safety precautions when working with chemical substances.

2-amino-4-methoxybenzaldehyde

59236-36-1: 2-Amino-4-methoxybenzaldehyde, with the CAS number 59236-36-1, is an organic compound characterized by its aromatic structure featuring both an amino group and a methoxy group attached to a benzaldehyde moiety. This compound typically appears as a solid or crystalline substance and is known for its pale yellow to off-white color. It has a molecular formula that reflects the presence of an amino group (-NH2), a methoxy group (-OCH3), and an aldehyde group (-CHO), contributing to its reactivity and potential applications in organic synthesis. The amino group can participate in various reactions, such as nucleophilic substitutions, while the aldehyde group can undergo oxidation or condensation reactions. 2-Amino-4-methoxybenzaldehyde is often used in the synthesis of pharmaceuticals, agrochemicals, and dyes, owing to its functional groups that allow for further chemical modifications. Additionally, it may exhibit biological activity, making it of interest in medicinal chemistry. Proper handling and storage are essential due to its potential reactivity and the need for safety precautions when working with chemical substances.

CAS 59236-36-1

2-amino-4-methoxybenzaldehyde

2-amino-4-methoxy-benzaldehyde

Ref: IN-DA00EAIL

2-Amino-4-methoxybenzaldehyde

Ref: 54-OR310903