Nalpha-Fmoc-Nomega-(2,2,4,6,7-pentamethyl-2,3-dihydrobenzo[b]furan-5-ylsulfonyl)-L-beta-homoarginine

>95%

Reagent Code: #187796
label
Alias Fmoc-β-HoArg(Pbf)-OH;N-fluorene methoxycarbonyl-N'-(2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl)-L-Horacinine
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CAS Number 401915-53-5
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Properties Slightly soluble in water

science Other reagents with same CAS 401915-53-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 662.8 g/mol
Formula C₃₅H₄₂N₄O₇S
badge Registry Numbers
MDL Number MFCD03788172
inventory_2 Storage & Handling
Density 1.35±0.1 g/cm3
Storage -20°C, sealed, dry

description Product Description

Used in solid-phase peptide synthesis as a protected amino acid building block. The Fmoc group allows for mild base deprotection, compatible with standard Fmoc strategies, while the omega-sulfonyl group protects the guanidine moiety of homoarginine, preventing side reactions during coupling. The 2,2,4,6,7-pentamethyl-2,3-dihydrobenzo[b]furan-5-ylsulfonyl (Pbf-like) protecting group is stable during synthesis but can be removed during final acidic cleavage, making it suitable for use in complex peptide assembly. This compound is particularly useful in the preparation of bioactive peptides where precise modification and protection of the arginine side chain are critical.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,160.00
inventory 5g
10-20 days ฿14,850.00
inventory 10g
10-20 days ฿27,640.00
inventory 25g
10-20 days ฿59,430.00
Nalpha-Fmoc-Nomega-(2,2,4,6,7-pentamethyl-2,3-dihydrobenzo[b]furan-5-ylsulfonyl)-L-beta-homoarginine
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Used in solid-phase peptide synthesis as a protected amino acid building block. The Fmoc group allows for mild base deprotection, compatible with standard Fmoc strategies, while the omega-sulfonyl group protects the guanidine moiety of homoarginine, preventing side reactions during coupling. The 2,2,4,6,7-pentamethyl-2,3-dihydrobenzo[b]furan-5-ylsulfonyl (Pbf-like) protecting group is stable during synthesis but can be removed during final acidic cleavage, making it suitable for use in complex peptide assembly. This compound is particularly useful in the preparation of bioactive peptides where precise modification and protection of the arginine side chain are critical.
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