(R)-2-((((9H-FLUOREN-9-YL)METHOXY)CARBONYL)(METHYL)AMINO)-5-(TERT-BUTOXY)-5-OXOPENTANOIC ACID

98%

Reagent Code: #231099
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CAS Number 1562442-35-6

science Other reagents with same CAS 1562442-35-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 439.51 g/mol
Formula C₂₅H₂₉NO₆
badge Registry Numbers
MDL Number MFCD04974254
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used primarily in peptide synthesis as a protected chiral building block. Its main application lies in the preparation of complex peptides and peptidomimetics, where the tert-butoxy and Fmoc groups provide orthogonal protection for carboxylic acid and amine functionalities. The compound enables stepwise assembly of peptide chains with stereochemical control, making it valuable in pharmaceutical research and development, especially in synthesizing bioactive peptides with high purity and defined configuration. Commonly employed in solid-phase peptide synthesis (SPPS), it allows for mild deprotection conditions, preserving sensitive functional groups in the growing peptide chain.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,060.00
inventory 250mg
10-20 days ฿14,900.00
inventory 1g
10-20 days ฿20,230.00
(R)-2-((((9H-FLUOREN-9-YL)METHOXY)CARBONYL)(METHYL)AMINO)-5-(TERT-BUTOXY)-5-OXOPENTANOIC ACID
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Used primarily in peptide synthesis as a protected chiral building block. Its main application lies in the preparation of complex peptides and peptidomimetics, where the tert-butoxy and Fmoc groups provide orthogonal protection for carboxylic acid and amine functionalities. The compound enables stepwise assembly of peptide chains with stereochemical control, making it valuable in pharmaceutical research and development, especially in synthesizing bioactive peptides with high purity and defined configuration. Commonly employed in solid-phase peptide synthesis (SPPS), it allows for mild deprotection conditions, preserving sensitive functional groups in the growing peptide chain.
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