(2S)-N1-(2-Aminoethyl)-3-(4-ethoxyphenyl)-1,2-propanediamine trihydrochloride
[CAS# 221640-06-8]

Identification

• Classification: API
• Name: (2S)-N1-(2-Aminoethyl)-3-(4-ethoxyphenyl)-1,2-propanediamine trihydrochloride
• Synonyms: (2S)-1-N-(2-aminoethyl)-3-(4-ethoxyphenyl)propane-1,2-diamine;trihydrochloride
• Molecular Formula: C₁₃H₂₃N₃O^.3(HCl)
• Molecular Weight: 346.72
• CAS Registry Number: 221640-06-8
• EC Number: 811-169-2
• SMILES: CCOC1=CC=C(C=C1)C[C@@H](CNCCN)N.Cl.Cl.Cl

Safety Data

• Hazard Symbols: GHS07 Warning
• Hazard Statements: H302-H315-H319-H335
• Precautionary Statements: P261-P305+P351+P338

Discovory and Applicatios

(2S)-N1-(2-Aminoethyl)-3-(4-ethoxyphenyl)-1,2-propanediamine trihydrochloride is a chemical compound notable for its unique structure and diverse applications in chemistry and pharmaceuticals. This compound features a propanediamine backbone with aminoethyl and ethoxyphenyl substituents, and is presented as a trihydrochloride salt, which significantly impacts its solubility and reactivity.

The discovery of (2S)-N1-(2-aminoethyl)-3-(4-ethoxyphenyl)-1,2-propanediamine trihydrochloride is rooted in the need for versatile chemical entities with specific structural features for use in various applications. The synthesis of this compound involves the preparation of a chiral propanediamine derivative, followed by the introduction of an aminoethyl group and a 4-ethoxyphenyl substituent. The trihydrochloride salt form is then produced to enhance the solubility of the compound in aqueous solutions, which is crucial for its use in biological and chemical contexts.

In the field of pharmaceuticals, (2S)-N1-(2-aminoethyl)-3-(4-ethoxyphenyl)-1,2-propanediamine trihydrochloride is explored for its potential as a drug candidate. The compound’s structure allows for interactions with various biological targets, and its trihydrochloride salt form improves its bioavailability and pharmacokinetics. Research into this compound's efficacy and safety profiles is ongoing, with particular interest in its application as a therapeutic agent in treating conditions where selective interaction with biological targets is required.

In medicinal chemistry, the compound is studied for its role in designing and synthesizing novel drugs. Its functional groups, including the aminoethyl and ethoxyphenyl moieties, enable specific interactions with target molecules, which can be leveraged in drug design. The trihydrochloride salt form further aids in optimizing the compound’s delivery and stability, making it a valuable candidate for further development.

Additionally, (2S)-N1-(2-aminoethyl)-3-(4-ethoxyphenyl)-1,2-propanediamine trihydrochloride has potential applications in biochemical research. Its structure allows for the modulation of enzyme activity and receptor binding, which can be useful in studying biochemical pathways and developing assays for drug screening.

Overall, (2S)-N1-(2-aminoethyl)-3-(4-ethoxyphenyl)-1,2-propanediamine trihydrochloride represents a versatile compound with significant potential in pharmaceuticals and biochemical research. Its well-defined structure and the trihydrochloride form make it suitable for various applications, contributing to advancements in drug development and biochemical studies.