2-Azetidinemethanol, (S)-, with the CAS number 104587-62-4, is a chiral organic compound characterized by its azetidine ring structure, which is a four-membered cyclic amine. This compound features a hydroxymethyl group attached to the azetidine, contributing to its reactivity and potential applications in organic synthesis and medicinal chemistry. The (S)- designation indicates that it has a specific stereochemistry, which can influence its biological activity and interactions with other molecules. Typically, compounds like 2-Azetidinemethanol are studied for their potential as intermediates in the synthesis of pharmaceuticals or as building blocks in the development of more complex organic molecules. Its properties may include solubility in polar solvents, moderate stability under standard conditions, and the ability to participate in various chemical reactions, such as nucleophilic substitutions or cyclization processes. The study of such compounds is essential for understanding their role in drug design and development, particularly in the context of chirality and its effects on pharmacodynamics and pharmacokinetics.

2-Azetidinemethanol, (S)-

104587-62-4: 2-Azetidinemethanol, (S)-, with the CAS number 104587-62-4, is a chiral organic compound characterized by its azetidine ring structure, which is a four-membered cyclic amine. This compound features a hydroxymethyl group attached to the azetidine, contributing to its reactivity and potential applications in organic synthesis and medicinal chemistry. The (S)- designation indicates that it has a specific stereochemistry, which can influence its biological activity and interactions with other molecules. Typically, compounds like 2-Azetidinemethanol are studied for their potential as intermediates in the synthesis of pharmaceuticals or as building blocks in the development of more complex organic molecules. Its properties may include solubility in polar solvents, moderate stability under standard conditions, and the ability to participate in various chemical reactions, such as nucleophilic substitutions or cyclization processes. The study of such compounds is essential for understanding their role in drug design and development, particularly in the context of chirality and its effects on pharmacodynamics and pharmacokinetics.

CAS 104587-62-4

2-Azetidinemethanol, (S)-

(S)-2-AZETIDINEMETHANOL

Ref: IN-DA007GZE

(S)-Azetidine-2-methanol

Ref: 54-OR317201

(S)-Azetidin-2-ylmethanol

Ref: 10-F791570