(1S,4R)-cis-4-Amino-2-cyclopentene-1-methanol (CAS 136522-35-5)

(1S,4R)-cis-4-Amino-2-cyclopentene-1-methanol is a specialized organic compound featuring a cyclopentene ring substituted with amino and hydroxyl groups. This structure makes it an interesting molecule for various chemical and biochemical research areas, particularly in the study of cyclic amino alcohols and their derivatives. The compound′s cyclopentene core provides a rigid cyclic structure that is useful for probing stereochemical and conformational properties of cyclic systems. The presence of both amino and hydroxyl functional groups on this cyclopentene skeleton allows it to participate in a range of chemical reactions, making it a versatile intermediate in organic synthesis. In research, (1S,4R)-cis-4-Amino-2-cyclopentene-1-methanol is primarily utilized for its role in synthesizing more complex organic molecules. It serves as a building block in the synthesis of chiral ligands, pharmaceuticals, and other bioactive molecules. By modifying the amino and hydroxyl groups, chemists can produce a variety of derivatives with potential applications in catalysis, enzyme inhibition, and the synthesis of natural products. Moreover, this compound is used in studies focusing on asymmetric synthesis. The chiral centers at the 1S and 4R positions are particularly important for developing enantioselective synthetic routes, which are crucial for creating molecules with specific chirality. This aspect is key in the field of stereoselective synthesis, where the goal is to produce molecules with precise three-dimensional orientations.