(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(tert-butoxy)phenyl)-2-methylpropanoic acid

98%

Reagent Code: #233533
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CAS Number 1309873-74-2

science Other reagents with same CAS 1309873-74-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 473.56 g/mol
Formula C₂₉H₃₁NO₅
badge Registry Numbers
MDL Number MFCD32696669
thermostat Physical Properties
Boiling Point 661.1±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.204±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used primarily in peptide synthesis as a protected amino acid building block, this compound enables the preparation of complex peptides through solid-phase or solution-phase methods. Its Fmoc group allows for mild base-labile protection, facilitating stepwise elongation of peptide chains while preserving other sensitive functional groups. The tert-butoxy-phenyl and methyl substitutions provide steric bulk, useful for studying conformational effects in peptides or synthesizing sterically hindered analogs. Commonly applied in research settings for developing peptide-based drugs, probes, or biomaterials where precise stereochemistry and side-chain protection are critical.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,800.00
inventory 250mg
10-20 days ฿8,000.00
inventory 500mg
10-20 days ฿12,800.00
inventory 1g
10-20 days ฿19,200.00
inventory 10g
10-20 days ฿88,000.00
inventory 5g
10-20 days ฿56,000.00
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(tert-butoxy)phenyl)-2-methylpropanoic acid
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Used primarily in peptide synthesis as a protected amino acid building block, this compound enables the preparation of complex peptides through solid-phase or solution-phase methods. Its Fmoc group allows for mild base-labile protection, facilitating stepwise elongation of peptide chains while preserving other sensitive functional groups. The tert-butoxy-phenyl and methyl substitutions provide steric bulk, useful for studying conformational effects in peptides or synthesizing sterically hindered analogs.

Used primarily in peptide synthesis as a protected amino acid building block, this compound enables the preparation of complex peptides through solid-phase or solution-phase methods. Its Fmoc group allows for mild base-labile protection, facilitating stepwise elongation of peptide chains while preserving other sensitive functional groups. The tert-butoxy-phenyl and methyl substitutions provide steric bulk, useful for studying conformational effects in peptides or synthesizing sterically hindered analogs. Commonly applied in research settings for developing peptide-based drugs, probes, or biomaterials where precise stereochemistry and side-chain protection are critical.

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