(S)-2-((S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-phenylpropanamido)-3-phenylpropanoic acid
95%
- Product Code: 235037
CAS:
84889-09-8
| Molecular Weight: | 534.6 g./mol | Molecular Formula: | C₃₃H₃₀N₂O₅ |
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| EC Number: | MDL Number: | ||
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| Density: | Storage Condition: | Room temperature, dry |
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.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 50mg | 10-20 days | ฿180.00 |
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| 250mg | 10-20 days | ฿360.00 |
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| 1g | 10-20 days | ฿720.00 |
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| 5g | 10-20 days | ฿2,390.00 |
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| 25g | 10-20 days | ฿11,560.00 |
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(S)-2-((S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-phenylpropanamido)-3-phenylpropanoic acid
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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| Stable in pH range | - |
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