Fmoc-β-Homolys(Boc)-OH

≥97%

Reagent Code: #235137
label
Alias (3S)-7-[[(1,1-dimethylethoxy)carbonyl]amino]-3-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]heptanoic acid; (S)-3-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-7-((tert-butoxycarbonyl)amino)heptanoic acid; (S)-7-(Boc-amino)-3-(Fmoc-amino)heptanoic acid; Nβ-fluoren-methoxycarbonyl-Nω-tert-butoxycarbonyl-L-β-homolysine
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CAS Number 203854-47-1

science Other reagents with same CAS 203854-47-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 482.57 g/mol
Formula C₂₇H₃₄N₂O₆
badge Registry Numbers
MDL Number MFCD01863054
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in solid-phase peptide synthesis to incorporate a protected β-homo-lysine residue into peptide chains. The Fmoc group allows for mild base deprotection, compatible with standard Fmoc-SPPS protocols, while the Boc group protects the side-chain amine during synthesis. This building block is valuable for designing peptides with modified backbones, enhancing stability or altering biological activity. Commonly applied in research for developing peptidomimetics, enzyme substrates, and probes in chemical biology.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,830.00
inventory 250mg
10-20 days ฿3,090.00
inventory 1g
10-20 days ฿6,900.00
inventory 5g
10-20 days ฿30,500.00
Fmoc-β-Homolys(Boc)-OH
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Used in solid-phase peptide synthesis to incorporate a protected β-homo-lysine residue into peptide chains. The Fmoc group allows for mild base deprotection, compatible with standard Fmoc-SPPS protocols, while the Boc group protects the side-chain amine during synthesis. This building block is valuable for designing peptides with modified backbones, enhancing stability or altering biological activity. Commonly applied in research for developing peptidomimetics, enzyme substrates, and probes in chemical b

Used in solid-phase peptide synthesis to incorporate a protected β-homo-lysine residue into peptide chains. The Fmoc group allows for mild base deprotection, compatible with standard Fmoc-SPPS protocols, while the Boc group protects the side-chain amine during synthesis. This building block is valuable for designing peptides with modified backbones, enhancing stability or altering biological activity. Commonly applied in research for developing peptidomimetics, enzyme substrates, and probes in chemical biology.

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