Boc-Ser(Tos)-OMe
98%
- Product Code: 66140
CAS:
56926-94-4
| Molecular Weight: | 373.42 g./mol | Molecular Formula: | C₁₆H₂₃NO₇S |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 74-75℃ | Boiling Point: | |
| Density: | 1.236 | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in peptide synthesis as a protected form of serine. The Boc (tert-butyloxycarbonyl) group safeguards the amino group, while the Tos (tosyl) group protects the hydroxyl side chain of serine, and the OMe (methyl ester) group protects the carboxyl group. This protection allows for selective reactions during the stepwise construction of peptides, ensuring that the serine residue remains intact until the desired stage of synthesis. It is particularly useful in solid-phase peptide synthesis (SPPS) and other methods where precise control over amino acid reactivity is required. After the peptide chain is assembled, the protecting groups can be removed to yield the final peptide product.
Product Specification:
| Test | Specification |
|---|---|
| CARBON BY ELEMENTAL ANALYSIS | 50-51.5 |
| OXYGEN BY ELEMENTAL ANALYSIS | 29-30.5 |
| PURITY HPLC | 98-100 |
| INFRARED SPECTROMETRY | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿950.00 |
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| 5.000 | 10-20 days | ฿2,980.00 |
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Boc-Ser(Tos)-OMe
This chemical is primarily used in peptide synthesis as a protected form of serine. The Boc (tert-butyloxycarbonyl) group safeguards the amino group, while the Tos (tosyl) group protects the hydroxyl side chain of serine, and the OMe (methyl ester) group protects the carboxyl group. This protection allows for selective reactions during the stepwise construction of peptides, ensuring that the serine residue remains intact until the desired stage of synthesis. It is particularly useful in solid-phase peptide synthesis (SPPS) and other methods where precise control over amino acid reactivity is required. After the peptide chain is assembled, the protecting groups can be removed to yield the final peptide product.
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