Boc-Cys(Me)-OH
96%
- Product Code: 104219
CAS:
16947-80-1
| Molecular Weight: | 235.30 g./mol | Molecular Formula: | C₉H₁₇NO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00076923 | |
| Melting Point: | Boiling Point: | 388.7°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in peptide synthesis as a protected form of cysteine. The Boc (tert-butyloxycarbonyl) group serves as a protective group for the amino function, while the methyl group on the thiol side chain provides additional stability during the synthesis process. It is particularly useful in solid-phase peptide synthesis (SPPS) to prevent unwanted side reactions and ensure the correct formation of peptide bonds. The compound is also employed in the preparation of cysteine-containing peptides for research in biochemistry and pharmaceuticals, where precise control over the peptide structure is essential. Its application extends to the development of peptide-based drugs, where protecting groups are crucial for maintaining the integrity of the peptide chain during synthesis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $39.31 |
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| 1.000 | 10-20 days | $95.52 |
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| 5.000 | 10-20 days | $346.17 |
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Boc-Cys(Me)-OH
This chemical is primarily used in peptide synthesis as a protected form of cysteine. The Boc (tert-butyloxycarbonyl) group serves as a protective group for the amino function, while the methyl group on the thiol side chain provides additional stability during the synthesis process. It is particularly useful in solid-phase peptide synthesis (SPPS) to prevent unwanted side reactions and ensure the correct formation of peptide bonds. The compound is also employed in the preparation of cysteine-containing peptides for research in biochemistry and pharmaceuticals, where precise control over the peptide structure is essential. Its application extends to the development of peptide-based drugs, where protecting groups are crucial for maintaining the integrity of the peptide chain during synthesis.
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