(S)-3-(((Benzyloxy)carbonyl)amino)-4-phenylbutanoic acid

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Reagent Code: #38371
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CAS Number 26250-86-2

science Other reagents with same CAS 26250-86-2

blur_circular Chemical Specifications

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Weight 313.3478 g/mol
Formula C₁₈H₁₉NO₄
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This compound is primarily utilized in the synthesis of peptides and pharmaceutical intermediates. It serves as a key building block in the preparation of biologically active molecules, particularly in the development of enzyme inhibitors and receptor modulators. Its structure, featuring both a benzyloxycarbonyl protecting group and a phenylbutanoic acid moiety, makes it valuable in organic synthesis for creating complex molecules with specific stereochemistry. Additionally, it is employed in research settings for studying enzyme-substrate interactions and designing drug candidates targeting various diseases, including cancer and neurological disorders. Its application extends to medicinal chemistry, where it aids in optimizing drug potency and selectivity.

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inventory 1g
10-20 days ฿2,475.00

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(S)-3-(((Benzyloxy)carbonyl)amino)-4-phenylbutanoic acid
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This compound is primarily utilized in the synthesis of peptides and pharmaceutical intermediates. It serves as a key building block in the preparation of biologically active molecules, particularly in the development of enzyme inhibitors and receptor modulators. Its structure, featuring both a benzyloxycarbonyl protecting group and a phenylbutanoic acid moiety, makes it valuable in organic synthesis for creating complex molecules with specific stereochemistry. Additionally, it is employed in research setti
This compound is primarily utilized in the synthesis of peptides and pharmaceutical intermediates. It serves as a key building block in the preparation of biologically active molecules, particularly in the development of enzyme inhibitors and receptor modulators. Its structure, featuring both a benzyloxycarbonyl protecting group and a phenylbutanoic acid moiety, makes it valuable in organic synthesis for creating complex molecules with specific stereochemistry. Additionally, it is employed in research settings for studying enzyme-substrate interactions and designing drug candidates targeting various diseases, including cancer and neurological disorders. Its application extends to medicinal chemistry, where it aids in optimizing drug potency and selectivity.
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