BOC-L-PHE-OME
98%
- Product Code: 58031
Alias:
N-tert-butoxycarbonyl-L-phenylalanine methyl ester Boc-L-phenylalanine methyl ester BOC-L-L-phenylalanine methyl ester N-BOC-L-phenylalanine methyl ester N-BOC -L-Phenylalanine methyl ester
CAS:
51987-73-6
| Molecular Weight: | 279.33 g./mol | Molecular Formula: | C₁₅H₂₁NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00076977 | |
| Melting Point: | 36-40 °C | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
BOC-L-PHE-OME is widely used in peptide synthesis as a protected amino acid derivative. It serves as a crucial building block in the production of peptides, ensuring the selective reactivity of the amino group during coupling reactions. The BOC (tert-butoxycarbonyl) group protects the amino functionality, while the methyl ester (OME) protects the carboxyl group, allowing for controlled stepwise peptide chain assembly. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it helps achieve high purity and yield of the target peptides. Its stability and ease of deprotection make it a preferred choice in pharmaceutical research and the development of peptide-based drugs. Additionally, it is utilized in the study of peptide structure-activity relationships and in the synthesis of bioactive peptides for therapeutic applications.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 98-100 |
| MP | 36-40 |
| APPEARANCE | White to off white powder |
| NOTE: | This product is low melting point solid,may change state in different environments (solid, liquid or semi-solid) |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿290.00 |
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| 5.000 | 10-20 days | ฿520.00 |
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| 25.000 | 10-20 days | ฿1,720.00 |
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| 100.000 | 10-20 days | ฿6,580.00 |
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BOC-L-PHE-OME
BOC-L-PHE-OME is widely used in peptide synthesis as a protected amino acid derivative. It serves as a crucial building block in the production of peptides, ensuring the selective reactivity of the amino group during coupling reactions. The BOC (tert-butoxycarbonyl) group protects the amino functionality, while the methyl ester (OME) protects the carboxyl group, allowing for controlled stepwise peptide chain assembly. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it helps achieve high purity and yield of the target peptides. Its stability and ease of deprotection make it a preferred choice in pharmaceutical research and the development of peptide-based drugs. Additionally, it is utilized in the study of peptide structure-activity relationships and in the synthesis of bioactive peptides for therapeutic applications.
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