Boc-Tyr-OMe
99%
Reagent
Code: #104812
Alias
BOC-L-tyrosine methyl ester ; N-tert-butoxycarbonyl-L-tyrosine methyl ester
CAS Number
4326-36-7
blur_circular Chemical Specifications
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Molecular Information
Weight
295.33 g/mol
Formula
C₁₅H₂₁NO₅
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Registry Numbers
MDL Number
MFCD00191181
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Physical Properties
Melting Point
100-104 °C(lit.)
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Storage & Handling
Storage
Room temperature, dry, sealed
description Product Description
Boc-Tyr-OMe is widely used in peptide synthesis as a protected tyrosine derivative. It serves as a building block in the construction of larger peptide chains, where the Boc (tert-butoxycarbonyl) group protects the amino functionality during the synthesis process. This allows for selective deprotection and coupling reactions, enabling the precise assembly of peptides. It is particularly valuable in solid-phase peptide synthesis (SPPS), where stepwise addition of amino acids is required. Additionally, Boc-Tyr-OMe is employed in research and development of pharmaceuticals, especially in the study of peptide-based drugs and bioactive compounds. Its stability and ease of handling make it a preferred choice in organic and medicinal chemistry laboratories.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Melting Point | 100-108 |
Purity (HPLC) | 99-100 |
Specific Rotation [α]20/D (C=1, CHCl3) | 48-54 |
Appearance | White To Light Yellow Powder |
Infrared Spectrum | Conforms To Structure |
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Boc-Tyr-OMe
Boc-Tyr-OMe is widely used in peptide synthesis as a protected tyrosine derivative. It serves as a building block in the construction of larger peptide chains, where the Boc (tert-butoxycarbonyl) group protects the amino functionality during the synthesis process. This allows for selective deprotection and coupling reactions, enabling the precise assembly of peptides. It is particularly valuable in solid-phase peptide synthesis (SPPS), where stepwise addition of amino acids is required. Additionally, Boc-Tyr-OMe is employed in research and development of pharmaceuticals, especially in the study of peptide-based drugs and bioactive compounds. Its stability and ease of handling make it a preferred choice in organic and medicinal chemistry laboratories.
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