Boc-L-Tyr(2-Br-Z)-OH

98%

  • Product Code: 66136
  CAS:    47689-67-8
Molecular Weight: 494.33 g./mol Molecular Formula: C₂₂H₂₄BrNO₇
EC Number: MDL Number: MFCD00037098
Melting Point: 112-115 °C Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: Used in peptide synthesis as a protected amino acid derivative, it plays a crucial role in the production of complex peptides and proteins. The Boc (tert-butyloxycarbonyl) group protects the amine functionality, while the 2-Br-Z (2-bromobenzyloxycarbonyl) group safeguards the hydroxyl group of tyrosine. This dual protection allows for selective deprotection and coupling steps, enabling the precise construction of peptide chains. It is particularly valuable in solid-phase peptide synthesis (SPPS), where controlled reactions are essential for creating peptides with specific sequences. Its application extends to research in biochemistry, pharmaceuticals, and biotechnology, aiding in the development of therapeutic peptides, enzyme inhibitors, and other bioactive molecules.
Product Specification:
Test Specification
Melting point 112-115
PURITYHPLC 98-100
A20DC1METHANOL 6-10
APPEARANCE White to off-white powder
INFRARED SPECTROMETRY Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿400.00
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-
5.000 10-20 days ฿1,350.00
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-
Boc-L-Tyr(2-Br-Z)-OH
Used in peptide synthesis as a protected amino acid derivative, it plays a crucial role in the production of complex peptides and proteins. The Boc (tert-butyloxycarbonyl) group protects the amine functionality, while the 2-Br-Z (2-bromobenzyloxycarbonyl) group safeguards the hydroxyl group of tyrosine. This dual protection allows for selective deprotection and coupling steps, enabling the precise construction of peptide chains. It is particularly valuable in solid-phase peptide synthesis (SPPS), where controlled reactions are essential for creating peptides with specific sequences. Its application extends to research in biochemistry, pharmaceuticals, and biotechnology, aiding in the development of therapeutic peptides, enzyme inhibitors, and other bioactive molecules.
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