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
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
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
5.000 10-20 days $19.02
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-
25.000 10-20 days $72.70
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100.000 10-20 days $246.00
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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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