Boc-Phe(2-Me)-OH
98%
- Product Code: 104745
Alias:
BOC-L-2-Methylphenylalanine
CAS:
114873-05-1
| Molecular Weight: | 279.33 g./mol | Molecular Formula: | C₁₅H₂₁NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00671390 | |
| Melting Point: | 113°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily used in peptide synthesis as a building block. It serves as a protected amino acid derivative, where the Boc (tert-butoxycarbonyl) group safeguards the amino functionality during the coupling process. The presence of the 2-methyl group on the phenylalanine side chain introduces steric and electronic effects, which can influence the peptide's structure, stability, and interactions. It is particularly valuable in the development of modified peptides for pharmaceutical research, enabling the creation of analogs with tailored properties for drug discovery, enzyme studies, and biochemical applications. Its use ensures precise control over peptide assembly, making it essential in the synthesis of complex peptide-based therapeutics and biomaterials.
Product Specification:
| Test | Specification |
|---|---|
| Purity (HPLC) | 98-100 |
| Appearance | White To Light Yellow Powder |
| Infrared Spectrometry | Conforms To Structure |
| Proton NMR Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,470.00 |
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| 5.000 | 10-20 days | ฿5,823.00 |
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Boc-Phe(2-Me)-OH
This compound is primarily used in peptide synthesis as a building block. It serves as a protected amino acid derivative, where the Boc (tert-butoxycarbonyl) group safeguards the amino functionality during the coupling process. The presence of the 2-methyl group on the phenylalanine side chain introduces steric and electronic effects, which can influence the peptide's structure, stability, and interactions. It is particularly valuable in the development of modified peptides for pharmaceutical research, enabling the creation of analogs with tailored properties for drug discovery, enzyme studies, and biochemical applications. Its use ensures precise control over peptide assembly, making it essential in the synthesis of complex peptide-based therapeutics and biomaterials.
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