2-[(Furan-2-ylmethyl)amino]ethanol, with the CAS number 4439-22-9, is an organic compound characterized by the presence of both an amino group and an alcohol functional group. This compound features a furan ring, which is a five-membered aromatic heterocycle containing oxygen, contributing to its unique chemical properties. The amino group (-NH2) is attached to a carbon chain that includes an ethanol moiety, which enhances its solubility in polar solvents. The presence of the furan ring can impart interesting reactivity, making it a potential candidate for various chemical reactions, including those involving electrophilic substitution or nucleophilic attack. Additionally, the compound may exhibit biological activity due to the presence of the furan and amino functionalities, which can interact with biological systems. Its structural characteristics suggest potential applications in pharmaceuticals, agrochemicals, or as a building block in organic synthesis. However, specific reactivity, stability, and safety data should be consulted for practical applications and handling.

2-[(furan-2-ylmethyl)amino]ethanol

4439-22-9: 2-[(Furan-2-ylmethyl)amino]ethanol, with the CAS number 4439-22-9, is an organic compound characterized by the presence of both an amino group and an alcohol functional group. This compound features a furan ring, which is a five-membered aromatic heterocycle containing oxygen, contributing to its unique chemical properties. The amino group (-NH2) is attached to a carbon chain that includes an ethanol moiety, which enhances its solubility in polar solvents. The presence of the furan ring can impart interesting reactivity, making it a potential candidate for various chemical reactions, including those involving electrophilic substitution or nucleophilic attack. Additionally, the compound may exhibit biological activity due to the presence of the furan and amino functionalities, which can interact with biological systems. Its structural characteristics suggest potential applications in pharmaceuticals, agrochemicals, or as a building block in organic synthesis. However, specific reactivity, stability, and safety data should be consulted for practical applications and handling.

CAS 4439-22-9

2-[(furan-2-ylmethyl)amino]ethanol

2-[(2-furylmethyl)amino]ethanol

Ref: IN-DA00DCNT

2-[(2-Furylmethyl)amino]ethanol

Ref: 10-F042944

3-[(Furan-2-ylmethyl)-amino]-propan-1-ol

Ref: 3D-EAA43922