(1S,2S)-Cbz epoxide, identified by its CAS number 128018-44-0, is a chiral epoxide compound characterized by its cyclic ether structure, which contains a three-membered ring featuring an oxygen atom. This compound is derived from the corresponding carbamate and is often utilized in organic synthesis due to its reactivity, particularly in nucleophilic ring-opening reactions. The (1S,2S) designation indicates the specific stereochemistry at the chiral centers, which can influence its reactivity and interactions with biological systems. Typically, epoxides are known for their strain due to the angle strain in the three-membered ring, making them reactive intermediates in various chemical transformations. (1S,2S)-Cbz epoxide may also exhibit properties such as solubility in organic solvents and potential applications in the synthesis of pharmaceuticals or agrochemicals. Its unique stereochemistry and reactivity profile make it a valuable compound in asymmetric synthesis and medicinal chemistry.

(1S,2S)-Cbz epoxide

128018-44-0: (2S,3S)-1,2-Epoxy-3-(Benzyloxycarbonyl-Amino)-4-Phenylbutane, (2S,3S)-1,2-Epoxy-3-(Cbz-Amino)-4-Phenylbutane, Benzyl [(1S)-1-((2S)-oxiran-2-yl)-2-phenylethyl]carbamate, Benzyl [(1S)-1-((2S)-oxiranyl)-2-phenylethyl]carbamate, Carbamic acid, (1-oxiranyl-2-phenylethyl)-, phenylmethyl ester, [S-(R*,R*)]-, Carbamic acid, N-[(1S)-1-[(2S)-2-oxiranyl]-2-phenylethyl]-, phenylmethyl ester, Carbamic acid, [(1S)-1-(2S)-oxiranyl-2-phenylethyl]-, phenylmethyl ester, Phenylmethyl N-[(1S)-1-[(2S)-2-oxiranyl]-2-phenylethyl]carbamate

Carbamic acid, N-[(1S)-1-[(2S)-2-oxiranyl]-2-phenylethyl]-, phenylmethyl ester

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CAS 128018-44-0: (1S,2S)-Cbz epoxide

Carbamic acid, N-[(1S)-1-[(2S)-2-oxiranyl]-2-phenylethyl]-, phenylmethyl ester

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(2S,3S)-1,2-Epoxy-3-(cbz-amino)-4-phenylbutane

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