CAS 24455-93-4

N-(4-methoxyphenyl)ethane-1,2-diamine

Description:

N-(4-methoxyphenyl)ethane-1,2-diamine, with the CAS number 24455-93-4, is an organic compound characterized by its amine functional groups and a methoxy-substituted aromatic ring. This compound features a two-carbon ethane backbone with amino groups (-NH2) at the first and second carbon positions, and a para-methoxy group (-OCH3) attached to the aromatic ring. The presence of the methoxy group enhances the compound's solubility in organic solvents and may influence its reactivity and biological activity. Typically, compounds like this can exhibit properties such as being a potential intermediate in organic synthesis or having applications in pharmaceuticals due to their ability to interact with biological systems. The molecular structure suggests that it may participate in hydrogen bonding, which can affect its physical properties, such as melting and boiling points. Additionally, the compound's stability and reactivity can be influenced by the electron-donating nature of the methoxy group, making it a subject of interest in various chemical research fields.

Formula: C₉H₁₄N₂O

InChI: InChI=1/C9H14N2O/c1-12-9-4-2-8(3-5-9)11-7-6-10/h2-5,11H,6-7,10H2,1H3

SMILES: COc1ccc(cc1)NCCN

Synonyms:

• 1,2-ethanediamine, N~1~-(4-methoxyphenyl)-
• N-(4-Methoxyphenyl)ethane-1,2-diamine

N-(4-Methoxyphenyl)ethane-1,2-diamine

CAS: 24455-93-4

Formula: C₉H₁₄N₂O

Purity: 95%

Color and Shape: Solid

Molecular weight: 166.2203

Ref: IN-DA006UY2

N1-(4-Methoxyphenyl)ethane-1,2-diamine

CAS: 24455-93-4

N1-(4-Methoxyphenyl)ethane-1,2-diamine

Purity: 95%

Molecular weight: 166.22g/mol

Ref: 54-OR1044699

N-(4-Methoxyphenyl)ethane-1,2-diamine

CAS: 24455-93-4

N-(4-Methoxyphenyl)ethane-1,2-diamine is a synthetic compound that has been shown to inhibit the activity of cathepsins. It can be used in the treatment of diseases caused by these enzymes, such as osteoarthritis and Alzheimer's disease. N-(4-Methoxyphenyl)ethane-1,2-diamine has a pharmacokinetic profile that is favorable for oral administration. The drug is absorbed from the gastrointestinal tract readily and undergoes extensive metabolism in the liver. This process leads to the formation of active metabolites which are excreted in urine or bile. N-(4-Methoxyphenyl)ethane-1,2-diamine also inhibits nitroalkanes with activated aromatic rings, such as 4-nitrobenzaldehyde and 2,4,6-trinitrobenzene.

Formula: C₉H₁₄N₂O

Purity: Min. 95%

Color and Shape: Slightly Yellow Powder

Molecular weight: 166.22 g/mol

Ref: 3D-FM122329

N-(4-methoxyphenyl)ethane-1,2-diamine

CAS: 24455-93-4

Formula: C₉H₁₄N₂O

Purity: 95%

Molecular weight: 166.224

Ref: 10-F369409