Boc-N-methyl-L-alanine

98%

  • Product Code: 104824
  Alias:    BOC-N-methyl-L-alanine
  CAS:    16948-16-6
Molecular Weight: 203.24 g./mol Molecular Formula: C₉H₁₇NO₄
EC Number: MDL Number: MFCD00037242
Melting Point: 88-92 °C Boiling Point:
Density: Storage Condition: room temperature
Product Description: Boc-N-methyl-L-alanine is widely used in peptide synthesis as a protecting group for amino acids. The Boc (tert-butyloxycarbonyl) group safeguards the amino functionality during the synthesis process, preventing unwanted side reactions. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it helps in the stepwise construction of peptides by ensuring selective deprotection and coupling reactions. Additionally, it is employed in the development of peptidomimetics and bioactive peptides, where the N-methyl group enhances metabolic stability and bioavailability. Its application extends to medicinal chemistry for designing peptide-based drugs and exploring structure-activity relationships.
Product Specification:
Test Specification
Melting Point 88-92
Purity (HPLC) 98-100
Specific Rotation [A]20/DC = 1 Ethanol 29-31
Appearance White To Light Yellow Powder
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days €9.50
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5.000 10-20 days €23.22
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25.000 10-20 days €111.86
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Boc-N-methyl-L-alanine
Boc-N-methyl-L-alanine is widely used in peptide synthesis as a protecting group for amino acids. The Boc (tert-butyloxycarbonyl) group safeguards the amino functionality during the synthesis process, preventing unwanted side reactions. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it helps in the stepwise construction of peptides by ensuring selective deprotection and coupling reactions. Additionally, it is employed in the development of peptidomimetics and bioactive peptides, where the N-methyl group enhances metabolic stability and bioavailability. Its application extends to medicinal chemistry for designing peptide-based drugs and exploring structure-activity relationships.
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