Understanding the detailed chemical profile of key intermediates is crucial for chemists engaged in synthesis and formulation. (S)-Boc-γ-Iodo-Abu-OMe, identified by CAS number 101650-14-0, is a valuable compound whose properties dictate its utility in various chemical reactions. This article explores its essential characteristics and provides insights relevant to its synthesis and application.

Chemically, (S)-Boc-γ-Iodo-Abu-OMe is recognized as methyl (2S)-4-iodo-2-[(2-methylpropan-2-yl)oxycarbonylamino]butanoate. Its molecular formula is C10H18INO4, with a molecular weight of approximately 343.16. Key physical properties include a density around 1.500±0.06 g/cm³, and it typically presents as a white to off-white solid. The compound’s LogP value of 2.0822 indicates moderate lipophilicity, and its PSA of 68.12 relates to its polarity. These parameters are vital for predicting solubility and behavior in different solvent systems during synthesis.

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The synthesis of such Boc-protected amino acid derivatives often involves careful protection strategies and functional group manipulations. While specific synthesis routes can vary, they typically begin with readily available amino acid precursors. The introduction of the Boc protecting group and the subsequent iodination at the gamma position are key steps. Availability from established suppliers means that chemists can focus on leveraging this intermediate rather than dedicating extensive resources to its preparation.

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