(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-cyclobutylaceticacid

98%

Reagent Code: #232157
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CAS Number 923012-41-3

science Other reagents with same CAS 923012-41-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 351.4 g/mol
Formula C₂₁H₂₁NO₄
badge Registry Numbers
MDL Number MFCD27951989
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in peptide synthesis as a chiral building block, this compound serves as a protected amino acid derivative that enables the controlled assembly of complex peptides. Its Fmoc group allows for mild base-labile protection, making it compatible with solid-phase synthesis strategies. The cyclobutyl moiety introduces conformational restraint, which can enhance selectivity and stability in the resulting peptides. It is especially valuable in the development of bioactive peptides and pharmaceutical agents where stereochemistry plays a critical role in biological activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,080.00
inventory 250mg
10-20 days ฿10,120.00
inventory 1g
10-20 days ฿27,430.00
(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-cyclobutylaceticacid
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Used primarily in peptide synthesis as a chiral building block, this compound serves as a protected amino acid derivative that enables the controlled assembly of complex peptides. Its Fmoc group allows for mild base-labile protection, making it compatible with solid-phase synthesis strategies. The cyclobutyl moiety introduces conformational restraint, which can enhance selectivity and stability in the resulting peptides. It is especially valuable in the development of bioactive peptides and pharmaceutica

Used primarily in peptide synthesis as a chiral building block, this compound serves as a protected amino acid derivative that enables the controlled assembly of complex peptides. Its Fmoc group allows for mild base-labile protection, making it compatible with solid-phase synthesis strategies. The cyclobutyl moiety introduces conformational restraint, which can enhance selectivity and stability in the resulting peptides. It is especially valuable in the development of bioactive peptides and pharmaceutical agents where stereochemistry plays a critical role in biological activity.

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