(1R)-1-Phenylprop-2-en-1-amine hydrochloride, with the CAS number 1181394-16-0, is a chemical compound characterized by its amine functional group and an alkenyl structure. This compound features a phenyl group attached to a propene backbone, which contributes to its reactivity and potential applications in organic synthesis and medicinal chemistry. As a hydrochloride salt, it is typically more stable and soluble in water compared to its free base form, making it easier to handle in laboratory settings. The presence of the amine group suggests that it may participate in various chemical reactions, such as nucleophilic substitutions or coupling reactions. Additionally, the stereochemistry indicated by the (1R) designation implies specific spatial arrangements that can influence the compound's biological activity and interactions with other molecules. Overall, this compound may be of interest in the development of pharmaceuticals or as a building block in organic synthesis due to its unique structural features.

(1R)-1-PHENYLPROP-2-EN-1-AMINE HCL

1181394-16-0: (1R)-1-Phenylprop-2-en-1-amine hydrochloride, with the CAS number 1181394-16-0, is a chemical compound characterized by its amine functional group and an alkenyl structure. This compound features a phenyl group attached to a propene backbone, which contributes to its reactivity and potential applications in organic synthesis and medicinal chemistry. As a hydrochloride salt, it is typically more stable and soluble in water compared to its free base form, making it easier to handle in laboratory settings. The presence of the amine group suggests that it may participate in various chemical reactions, such as nucleophilic substitutions or coupling reactions. Additionally, the stereochemistry indicated by the (1R) designation implies specific spatial arrangements that can influence the compound's biological activity and interactions with other molecules. Overall, this compound may be of interest in the development of pharmaceuticals or as a building block in organic synthesis due to its unique structural features.

CAS 1181394-16-0

(1R)-1-PHENYLPROP-2-EN-1-AMINE HCL

(R)-1-Phenylprop-2-en-1-amine hydrochloride

Ref: IN-DA01KK1A

(R)-1-Phenylprop-2-en-1-amine hydrochloride

Ref: 54-OR1058265