(S)-14-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-(tert-butoxycarbonyl)-2,2-dimethyl-4,8-dioxo-3,6-dioxa-5,9-diazapentadecan-15-oic acid

95%

Reagent Code: #232484
fingerprint
CAS Number 1008512-23-9

science Other reagents with same CAS 1008512-23-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 641.71 g/mol
Formula C₃₃H₄₃N₃O₁₀
badge Registry Numbers
MDL Number MFCD18427299
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in peptide synthesis as a protected amino acid building block, particularly in solid-phase synthesis. The Fmoc group provides temporary N-terminal protection that is easily removed under mild basic conditions, allowing stepwise assembly of peptides. The tert-butoxycarbonyl (Boc) group offers orthogonal protection for a secondary amine, enabling selective deprotection and coupling in complex peptide sequences. Its solubility in common organic solvents and stability during repeated synthesis cycles make it suitable for automated peptide synthesizers. Frequently employed in the preparation of long or branched peptides, including those used in pharmaceutical research and development.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,200.00
inventory 1g
10-20 days ฿37,570.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-14-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-(tert-butoxycarbonyl)-2,2-dimethyl-4,8-dioxo-3,6-dioxa-5,9-diazapentadecan-15-oic acid
No image available
Used in peptide synthesis as a protected amino acid building block, particularly in solid-phase synthesis. The Fmoc group provides temporary N-terminal protection that is easily removed under mild basic conditions, allowing stepwise assembly of peptides. The tert-butoxycarbonyl (Boc) group offers orthogonal protection for a secondary amine, enabling selective deprotection and coupling in complex peptide sequences. Its solubility in common organic solvents and stability during repeated synthesis cycles make it suitable for automated peptide synthesizers. Frequently employed in the preparation of long or branched peptides, including those used in pharmaceutical research and development.
Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...