Boc-L-serine benzyl ester
97%
- Product Code: 105537
Alias:
N-tert-butoxycarbonyl-L-serine
CAS:
59524-02-6
Molecular Weight: | 295.33 g./mol | Molecular Formula: | C₁₅H₂₁NO₅ |
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EC Number: | MDL Number: | MFCD00076983 | |
Melting Point: | 91 °C (dec.)(lit.) | Boiling Point: | |
Density: | Storage Condition: | 2~8°C |
Product Description:
Boc-L-serine benzyl ester is widely used in peptide synthesis as a protected form of serine. The Boc (tert-butoxycarbonyl) group safeguards the amino group, while the benzyl ester protects the carboxyl group, allowing selective reactions during peptide chain assembly. It is particularly valuable in solid-phase peptide synthesis (SPPS), where controlled deprotection and coupling steps are essential. This compound is also employed in the preparation of serine-containing peptides for pharmaceutical research, enabling the development of drug candidates, enzyme inhibitors, and bioactive peptides. Its stability and ease of removal under specific conditions make it a preferred choice in organic and medicinal chemistry.
Product Specification:
Test | Specification |
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Specific Rotation [A]20/D(C=2, H2O) | 7-10 |
Melting Point | 72-74 |
Purity (HPLC) | 97-100 |
300 MHz NMR Spectrum 1H | Conforms To Structure |
Appearance | White To Light Yellow Powder |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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5.000 | 10-20 days | $20.34 |
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25.000 | 10-20 days | $77.75 |
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100.000 | 10-20 days | $263.08 |
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Boc-L-serine benzyl ester
Boc-L-serine benzyl ester is widely used in peptide synthesis as a protected form of serine. The Boc (tert-butoxycarbonyl) group safeguards the amino group, while the benzyl ester protects the carboxyl group, allowing selective reactions during peptide chain assembly. It is particularly valuable in solid-phase peptide synthesis (SPPS), where controlled deprotection and coupling steps are essential. This compound is also employed in the preparation of serine-containing peptides for pharmaceutical research, enabling the development of drug candidates, enzyme inhibitors, and bioactive peptides. Its stability and ease of removal under specific conditions make it a preferred choice in organic and medicinal chemistry.
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