(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4,4-difluorocyclohexyl)propanoic acid

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Reagent Code: #232518
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CAS Number 2276607-04-4

science Other reagents with same CAS 2276607-04-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 429.46 g/mol
Formula C₂₄H₂₅F₂NO₄
badge Registry Numbers
MDL Number MFCD32661375
thermostat Physical Properties
Boiling Point 612.2±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.32±0.1 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used primarily in peptide synthesis as a protected amino acid building block, this compound enables the incorporation of a fluorinated cyclohexyl alanine derivative into peptide chains. The Fmoc group allows for mild base-labile protection, compatible with solid-phase synthesis, making it valuable in the preparation of structurally modified peptides for pharmaceutical and biochemical research. The difluorocyclohexyl moiety enhances metabolic stability and influences conformational preference, which can improve peptide binding affinity, bioavailability, or resistance to enzymatic degradation. It is particularly useful in the development of peptidomimetics and in structure-activity relationship (SAR) studies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿19,440.00
inventory 500mg
10-20 days ฿51,840.00
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4,4-difluorocyclohexyl)propanoic acid
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Used primarily in peptide synthesis as a protected amino acid building block, this compound enables the incorporation of a fluorinated cyclohexyl alanine derivative into peptide chains. The Fmoc group allows for mild base-labile protection, compatible with solid-phase synthesis, making it valuable in the preparation of structurally modified peptides for pharmaceutical and biochemical research. The difluorocyclohexyl moiety enhances metabolic stability and influences conformational preference, which can i

Used primarily in peptide synthesis as a protected amino acid building block, this compound enables the incorporation of a fluorinated cyclohexyl alanine derivative into peptide chains. The Fmoc group allows for mild base-labile protection, compatible with solid-phase synthesis, making it valuable in the preparation of structurally modified peptides for pharmaceutical and biochemical research. The difluorocyclohexyl moiety enhances metabolic stability and influences conformational preference, which can improve peptide binding affinity, bioavailability, or resistance to enzymatic degradation. It is particularly useful in the development of peptidomimetics and in structure-activity relationship (SAR) studies.

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