CAS 85612-60-8

(2S)-3-Phenyl-1,2-propanediamine

Description:

(2S)-3-Phenyl-1,2-propanediamine, with the CAS number 85612-60-8, is an organic compound characterized by its chiral structure, featuring two amine groups and a phenyl substituent. This compound is a derivative of propanediamine, where the second carbon in the chain is attached to a phenyl group, imparting unique properties. It exists as a colorless to pale yellow liquid or solid, depending on its form and purity. The presence of amine functional groups makes it basic and capable of forming salts with acids. Its chirality indicates that it can exist in two enantiomeric forms, with the (2S) configuration being one of them, which can influence its biological activity and interactions. This compound is of interest in medicinal chemistry and organic synthesis, often serving as a building block for more complex molecules. Additionally, it may exhibit properties such as solubility in polar solvents and potential reactivity in various chemical reactions, including nucleophilic substitutions and coupling reactions.

Formula: C₉H₁₄N₂

InChI: InChI=1S/C9H14N2/c10-7-9(11)6-8-4-2-1-3-5-8/h1-5,9H,6-7,10-11H2/t9-/m0/s1

InChI key: InChIKey=CXFFQOZYXJHZNJ-VIFPVBQESA-N

SMILES: C([C@@H](CN)N)C1=CC=CC=C1

Synonyms:

• (2S)-3-Phenyl-1,2-propanediamine
• (2S)-3-Phenylpropane-1,2-diamine
• (S)-3-Phenyl-1,2-propanediamine
• 1,2-Propanediamine,3-phenyl-, (S)-
• 1,2-Propanediamine, 3-phenyl-, (2S)-
• (S)-3-Phenylpropane-1,2-diamine

(2S)-3-Phenyl-1,2-propanediamine

Controlled Product

CAS: 85612-60-8

Applications An antibacterial agent.
References Brunner, H., et al.: Eur. J. Med. Chem., 25, 35 (1990),

Formula: C₉H₁₄N₂

Color and Shape: Neat

Molecular weight: 150.22

Ref: TR-P336080