(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-methyl-4-phenylpentanoic acid

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Reagent Code: #38052
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CAS Number 2350186-20-6

science Other reagents with same CAS 2350186-20-6

blur_circular Chemical Specifications

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Weight 429.5076 g/mol
Formula C₂₇H₂₇NO₄
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This compound is an Fmoc-protected derivative of (S)-2-amino-4-methyl-4-phenylpentanoic acid, serving as a specialized building block in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group protects the N-terminal amino group, allowing selective deprotection and precise stepwise incorporation of the unnatural amino acid residue into peptide chains without interfering with other functional groups. Its stability in basic conditions and easy removal under mild acidic conditions make it a valuable reagent in biochemical and pharmaceutical research for constructing peptides with tailored sequences and structures.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿8,064.00

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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-methyl-4-phenylpentanoic acid
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This compound is an Fmoc-protected derivative of (S)-2-amino-4-methyl-4-phenylpentanoic acid, serving as a specialized building block in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group protects the N-terminal amino group, allowing selective deprotection and precise stepwise incorporation of the unnatural amino acid residue into peptide chains without interfering with other functional groups. Its stability in basic conditions and easy removal under mild acidic conditions ma

This compound is an Fmoc-protected derivative of (S)-2-amino-4-methyl-4-phenylpentanoic acid, serving as a specialized building block in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group protects the N-terminal amino group, allowing selective deprotection and precise stepwise incorporation of the unnatural amino acid residue into peptide chains without interfering with other functional groups. Its stability in basic conditions and easy removal under mild acidic conditions make it a valuable reagent in biochemical and pharmaceutical research for constructing peptides with tailored sequences and structures.

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