N-(Triphenylmethyl)-L-serine Methyl Ester
99%
- Product Code: 76471
CAS:
4465-44-5
| Molecular Weight: | 361.44 g./mol | Molecular Formula: | C₂₃H₂₃NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00192570 | |
| Melting Point: | 148-150°C (Lit.) | Boiling Point: | |
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
N-(Triphenylmethyl)-L-serine Methyl Ester is primarily used in organic synthesis, particularly in peptide chemistry. It serves as a protected form of L-serine, where the triphenylmethyl (trityl) group shields the amino group, and the methyl ester protects the carboxyl group. This protection allows selective reactions to occur at other sites of the molecule without interference. It is commonly employed in the stepwise construction of peptides, ensuring the integrity of the serine residue during complex synthetic processes. Additionally, it is utilized in the development of pharmaceuticals and bioactive compounds, where precise control over amino acid reactivity is crucial. The compound’s stability and ease of deprotection make it a valuable tool in research and industrial applications.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 98.5 100% |
| Melting point | 146 150? |
| Specific rotation a20DC1MeOH | 31-35 |
| Appearance | White - Slightly pale yellow Crystal - Powder |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | $46.37 |
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| 25.000 | 10-20 days | $202.45 |
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N-(Triphenylmethyl)-L-serine Methyl Ester
N-(Triphenylmethyl)-L-serine Methyl Ester is primarily used in organic synthesis, particularly in peptide chemistry. It serves as a protected form of L-serine, where the triphenylmethyl (trityl) group shields the amino group, and the methyl ester protects the carboxyl group. This protection allows selective reactions to occur at other sites of the molecule without interference. It is commonly employed in the stepwise construction of peptides, ensuring the integrity of the serine residue during complex synthetic processes. Additionally, it is utilized in the development of pharmaceuticals and bioactive compounds, where precise control over amino acid reactivity is crucial. The compound’s stability and ease of deprotection make it a valuable tool in research and industrial applications.
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