CAS 16495-67-3

Isopropyl-(4-Methoxy-Phenyl)-Amine

Description:

Isopropyl-(4-Methoxy-Phenyl)-Amine, with the CAS number 16495-67-3, is an organic compound characterized by the presence of an isopropyl group and a para-methoxyphenyl amine structure. This compound typically exhibits properties associated with amines, such as basicity and the ability to form hydrogen bonds, which can influence its solubility in various solvents. The methoxy group contributes to its electronic properties, potentially enhancing its reactivity and interaction with biological systems. Isopropyl-(4-Methoxy-Phenyl)-Amine may be utilized in various chemical syntheses or as an intermediate in the production of pharmaceuticals and agrochemicals. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of compounds with specific biological activities. Safety data should be consulted for handling and storage, as amines can be hazardous. Overall, this compound represents a versatile building block in organic synthesis and medicinal chemistry.

Formula: C₁₀H₁₅NO

Synonyms:

• N-Iso-Propyl-4-Methoxyaniline
• N-Isopropyl-N-(4-methoxyphenyl)amine
• N-Isopropyl-4-methoxyaniline

4-methoxy-N-(propan-2-yl)aniline

CAS: 16495-67-3

Formula: C₁₀H₁₅NO

Purity: 97%

Color and Shape: Solid

Molecular weight: 165.2322

Ref: IN-DA001V6N

N-iso-Propyl-4-methoxyaniline

CAS: 16495-67-3

Formula: C₁₀H₁₅NO

Purity: 97%

Molecular weight: 165.236

Ref: 10-F020629

N-iso-Propyl-4-methoxyaniline

CAS: 16495-67-3

N-iso-Propyl-4-methoxyaniline is a supramolecular framework that has been demonstrated to be mediated by nitrogen atoms. This framework has been shown to form when the two isomers are mixed together, which leads to the formation of an alkylation reaction. The isomerism of this compound can be quantified and is unique in that it destabilizes the molecule. X-ray crystallography has been used to study the molecular structure and elucidate the non-covalent interactions. N-iso-Propyl-4-methoxyaniline's destabilization may be attributed to its ability to form hydrogen bonds with water molecules, as well as its hydrophobic character.

Formula: C₁₀H₁₅NO

Purity: Min. 95%

Molecular weight: 165.24 g/mol

Ref: 3D-RAA49567