(S)-2-((S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-phenylpropanamido)-3-phenylpropanoic acid

95%

Reagent Code: #235037
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CAS Number 84889-09-8

science Other reagents with same CAS 84889-09-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 534.6 g/mol
Formula C₃₃H₃₀N₂O₅
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Widely used in peptide synthesis, this compound serves as a key building block for introducing phenylalanine derivatives with stereochemical control. Its primary application lies in solid-phase peptide synthesis (SPPS), where the Fmoc group enables reversible protection of the amino terminus, allowing stepwise assembly of peptide chains. The chiral centers ensure stereoselective coupling, making it valuable for synthesizing enantiomerically pure peptides used in pharmaceutical research and development. It is especially useful in the preparation of bioactive peptides and peptidomimetics where precise spatial arrangement of side chains is critical for activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿180.00
inventory 250mg
10-20 days ฿360.00
inventory 1g
10-20 days ฿720.00
inventory 5g
10-20 days ฿2,390.00
inventory 25g
10-20 days ฿11,560.00
(S)-2-((S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-phenylpropanamido)-3-phenylpropanoic acid
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Widely used in peptide synthesis, this compound serves as a key building block for introducing phenylalanine derivatives with stereochemical control. Its primary application lies in solid-phase peptide synthesis (SPPS), where the Fmoc group enables reversible protection of the amino terminus, allowing stepwise assembly of peptide chains. The chiral centers ensure stereoselective coupling, making it valuable for synthesizing enantiomerically pure peptides used in pharmaceutical research and development. I

Widely used in peptide synthesis, this compound serves as a key building block for introducing phenylalanine derivatives with stereochemical control. Its primary application lies in solid-phase peptide synthesis (SPPS), where the Fmoc group enables reversible protection of the amino terminus, allowing stepwise assembly of peptide chains. The chiral centers ensure stereoselective coupling, making it valuable for synthesizing enantiomerically pure peptides used in pharmaceutical research and development. It is especially useful in the preparation of bioactive peptides and peptidomimetics where precise spatial arrangement of side chains is critical for activity.

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