(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-((acetamidomethyl)thio)butanoic acid
98%
- Product Code: 236512
CAS:
150281-21-3
| Molecular Weight: | 428.50 g./mol | Molecular Formula: | C₂₂H₂₄N₂O₅S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03788052 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry |
Product Description:
Used in peptide synthesis as a protected amino acid derivative, particularly for introducing cysteine-like residues with modified sulfur functionality. The acetamidomethyl (Acm) group protects the thiol side chain, allowing selective deprotection and disulfide bond formation in complex peptide assembly. The Fmoc group enables solid-phase synthesis by providing orthogonal protection for the alpha-amino group, compatible with base-labile cleavage conditions. Commonly applied in the preparation of structured peptides requiring precise disulfide bridge pairing, such as in therapeutic peptides or cyclic peptide scaffolds.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿8,400.00 |
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| 250mg | 10-20 days | ฿12,100.00 |
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| 1g | 10-20 days | ฿35,910.00 |
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-((acetamidomethyl)thio)butanoic acid
Used in peptide synthesis as a protected amino acid derivative, particularly for introducing cysteine-like residues with modified sulfur functionality. The acetamidomethyl (Acm) group protects the thiol side chain, allowing selective deprotection and disulfide bond formation in complex peptide assembly. The Fmoc group enables solid-phase synthesis by providing orthogonal protection for the alpha-amino group, compatible with base-labile cleavage conditions. Commonly applied in the preparation of structured peptides requiring precise disulfide bridge pairing, such as in therapeutic peptides or cyclic peptide scaffolds.
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| Stable in pH range | - |
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