(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-4-(tert-butoxy)-4-oxobutanoic acid
95%
- Product Code: 231267
CAS:
1799443-40-5
| Molecular Weight: | 425.47 g./mol | Molecular Formula: | C₂₄H₂₇NO₆ |
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| Density: | Storage Condition: | 2-8°C, dry |
Product Description:
Widely used in peptide synthesis, this compound serves as a chiral building block for introducing protected glutamic acid derivatives with high stereochemical purity. Its Fmoc group allows for mild base-labile protection, making it compatible with solid-phase peptide synthesis (SPPS). The tert-butyl ester offers orthogonal protection for the side chain carboxylic acid, enabling selective deprotection under acidic conditions without affecting the Fmoc group. This dual protection strategy is essential for the stepwise assembly of complex peptides, especially in pharmaceutical research and development of bioactive molecules.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿5,200.00 |
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| 250mg | 10-20 days | ฿8,770.00 |
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| 1g | 10-20 days | ฿27,980.00 |
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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-4-(tert-butoxy)-4-oxobutanoic acid
Widely used in peptide synthesis, this compound serves as a chiral building block for introducing protected glutamic acid derivatives with high stereochemical purity. Its Fmoc group allows for mild base-labile protection, making it compatible with solid-phase peptide synthesis (SPPS). The tert-butyl ester offers orthogonal protection for the side chain carboxylic acid, enabling selective deprotection under acidic conditions without affecting the Fmoc group. This dual protection strategy is essential for the stepwise assembly of complex peptides, especially in pharmaceutical research and development of bioactive molecules.
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