(2S,3S)-2-((2S,3S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-methylpentanamido)-3-methylpentanoic acid

97%

Reagent Code: #232420
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CAS Number 2171279-24-4

science Other reagents with same CAS 2171279-24-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 466.57 g/mol
Formula C₂₇H₃₄N₂O₅
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Widely used in peptide synthesis, this compound serves as a protected dipeptide building block, enabling stepwise assembly of complex peptides with high stereochemical control. The Fmoc group allows for mild base-labile protection of the amine, compatible with solid-phase synthesis, while the carboxylic acid can be activated for amide bond formation. Its branched alkyl side chains help modulate peptide solubility and conformational stability. Commonly employed in the preparation of structured peptides, enzyme substrates, and peptidomimetics for pharmaceutical research.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,270.00
(2S,3S)-2-((2S,3S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-methylpentanamido)-3-methylpentanoic acid
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Widely used in peptide synthesis, this compound serves as a protected dipeptide building block, enabling stepwise assembly of complex peptides with high stereochemical control. The Fmoc group allows for mild base-labile protection of the amine, compatible with solid-phase synthesis, while the carboxylic acid can be activated for amide bond formation. Its branched alkyl side chains help modulate peptide solubility and conformational stability. Commonly employed in the preparation of structured peptides, e

Widely used in peptide synthesis, this compound serves as a protected dipeptide building block, enabling stepwise assembly of complex peptides with high stereochemical control. The Fmoc group allows for mild base-labile protection of the amine, compatible with solid-phase synthesis, while the carboxylic acid can be activated for amide bond formation. Its branched alkyl side chains help modulate peptide solubility and conformational stability. Commonly employed in the preparation of structured peptides, enzyme substrates, and peptidomimetics for pharmaceutical research.

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