(S)-Ethyl 4-((tert-butoxycarbonyl)amino)-4-phenylbutanoate

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Reagent Code: #38491
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CAS Number 296778-55-7

science Other reagents with same CAS 296778-55-7

blur_circular Chemical Specifications

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Weight 307.3847 g/mol
Formula C₁₇H₂₅NO₄
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description Product Description

This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the development of chiral molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a phenyl moiety, makes it valuable in peptide synthesis and the production of enantiomerically pure compounds. It is often employed in the preparation of active pharmaceutical ingredients (APIs) for drugs targeting neurological and cardiovascular disorders. Additionally, its chiral center allows for the creation of stereospecific compounds, which are crucial in drug design to ensure efficacy and reduce side effects. It is also utilized in research for developing new therapeutic agents and studying biochemical pathways.

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inventory 100mg
10-20 days ฿8,343.00

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(S)-Ethyl 4-((tert-butoxycarbonyl)amino)-4-phenylbutanoate
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This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the development of chiral molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a phenyl moiety, makes it valuable in peptide synthesis and the production of enantiomerically pure compounds. It is often employed in the preparation of active pharmaceutical ingredients (APIs) for drugs targeting neurological and cardiovascular disorders. Additionally, its chiral center allows for

This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the development of chiral molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a phenyl moiety, makes it valuable in peptide synthesis and the production of enantiomerically pure compounds. It is often employed in the preparation of active pharmaceutical ingredients (APIs) for drugs targeting neurological and cardiovascular disorders. Additionally, its chiral center allows for the creation of stereospecific compounds, which are crucial in drug design to ensure efficacy and reduce side effects. It is also utilized in research for developing new therapeutic agents and studying biochemical pathways.

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