(2S)-2-Aminobut-3-en-1-ol hydrochloride is a chemical compound characterized by its amino alcohol structure, which features both an amine and an alcohol functional group. The "2S" designation indicates that it has a specific stereochemistry, making it a chiral molecule. The presence of the double bond in the but-3-en portion of the molecule contributes to its reactivity and potential applications in organic synthesis. As a hydrochloride salt, it is typically more stable and soluble in water compared to its free base form, which is advantageous for various applications, including pharmaceutical formulations. This compound may exhibit biological activity due to its amino and hydroxyl groups, potentially interacting with biological systems. Its CAS number, 219803-57-3, allows for precise identification in chemical databases. Overall, (2S)-2-Aminobut-3-en-1-ol hydrochloride is of interest in medicinal chemistry and may serve as a building block for more complex molecules.

(2S)-2-Aminobut-3-en-1-ol hydrochloride (1:1)

219803-57-3: 3-Buten-1-ol, 2-amino-, (2S)-, hydrochloride (1:1), (2S)-1-hydroxybut-3-en-2-aminium chloride, (S)-2-Amino-But-3-En-1-Ol Hydrochloride

CAS 219803-57-3: (2S)-2-Aminobut-3-en-1-ol hydrochloride (1:1)

(S)-2-Aminobut-3-en-1-ol hydrochloride

Ref: 54-OR92188

(S)-2-Aminobut-3-en-1-ol Hydrochloride

Ref: TR-A602130

(S)-2-AMINO-BUT-3-EN-1-OL HYDROCHLORIDE

Ref: IN-DA00BDFE

(S)-2-Amino-but-3-en-1-ol hydrochloride

Ref: 10-F040047