(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-6-(isopropylamino)hexanoic acid

98%

Reagent Code: #233352
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CAS Number 871811-39-1

science Other reagents with same CAS 871811-39-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 410.51 g/mol
Formula C₂₄H₃₀N₂O₄
badge Registry Numbers
MDL Number MFCD20489011
thermostat Physical Properties
Boiling Point 618.7±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.169±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used primarily in peptide synthesis as a chiral building block, this compound enables the incorporation of a protected amino acid with a branched aliphatic side chain. Its Fmoc group allows for mild base-labile protection, making it compatible with solid-phase peptide synthesis (SPPS). The isopropylamino group provides structural diversity, useful in designing peptides with enhanced stability or specific biological activity. Commonly applied in the preparation of enzyme inhibitors, peptidomimetics, and bioactive molecules in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿103,200.00
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-6-(isopropylamino)hexanoic acid
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Used primarily in peptide synthesis as a chiral building block, this compound enables the incorporation of a protected amino acid with a branched aliphatic side chain. Its Fmoc group allows for mild base-labile protection, making it compatible with solid-phase peptide synthesis (SPPS). The isopropylamino group provides structural diversity, useful in designing peptides with enhanced stability or specific biological activity. Commonly applied in the preparation of enzyme inhibitors, peptidomimetics, and b

Used primarily in peptide synthesis as a chiral building block, this compound enables the incorporation of a protected amino acid with a branched aliphatic side chain. Its Fmoc group allows for mild base-labile protection, making it compatible with solid-phase peptide synthesis (SPPS). The isopropylamino group provides structural diversity, useful in designing peptides with enhanced stability or specific biological activity. Commonly applied in the preparation of enzyme inhibitors, peptidomimetics, and bioactive molecules in medicinal chemistry research.

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