2,5-Dioxopyrrolidin-1-yl 1-(9H-fluoren-9-yl)-3-oxo-2,7,10,13,16-pentaoxa-4-azanonadecan-19-oate

95%

Reagent Code: #178054
fingerprint
CAS Number 1314378-14-7

science Other reagents with same CAS 1314378-14-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 584.61 g/mol
Formula C₃₀H₃₆N₂O₁₀
badge Registry Numbers
MDL Number MFCD20227659
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used primarily as an active ester in peptide synthesis, this compound enables efficient coupling of amino acids by enhancing the reactivity of carboxyl groups. It is especially valuable in solid-phase peptide synthesis where the fluorenylmethyloxycarbonyl (Fmoc) protecting group is employed, allowing for mild deprotection conditions. The polyether chain improves solubility in polar solvents, facilitating reactions in aqueous or mixed solvent systems. Its structure supports the synthesis of complex peptides and peptidomimetics used in pharmaceutical research and development.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿600.00
inventory 250mg
10-20 days ฿1,450.00
inventory 1g
10-20 days ฿5,710.00
inventory 5g
10-20 days ฿24,670.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2,5-Dioxopyrrolidin-1-yl 1-(9H-fluoren-9-yl)-3-oxo-2,7,10,13,16-pentaoxa-4-azanonadecan-19-oate
No image available

Used primarily as an active ester in peptide synthesis, this compound enables efficient coupling of amino acids by enhancing the reactivity of carboxyl groups. It is especially valuable in solid-phase peptide synthesis where the fluorenylmethyloxycarbonyl (Fmoc) protecting group is employed, allowing for mild deprotection conditions. The polyether chain improves solubility in polar solvents, facilitating reactions in aqueous or mixed solvent systems. Its structure supports the synthesis of complex peptid

Used primarily as an active ester in peptide synthesis, this compound enables efficient coupling of amino acids by enhancing the reactivity of carboxyl groups. It is especially valuable in solid-phase peptide synthesis where the fluorenylmethyloxycarbonyl (Fmoc) protecting group is employed, allowing for mild deprotection conditions. The polyether chain improves solubility in polar solvents, facilitating reactions in aqueous or mixed solvent systems. Its structure supports the synthesis of complex peptides and peptidomimetics 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...