(2s)-2-[(benzyloxy)carbonyl]amino-3-(3,4-dihydroxyphenyl)propanoic acid
98%
- Product Code: 233597
CAS:
30033-25-1
| Molecular Weight: | 331.32 g./mol | Molecular Formula: | C₁₇H₁₇NO₆ |
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| Density: | Storage Condition: | Room temperature |
Product Description:
Widely used in peptide synthesis as a protected form of L-DOPA, enabling the controlled assembly of complex peptides without unwanted side reactions at the catechol group. The benzyloxycarbonyl (Cbz) protecting group allows for selective deprotection under mild conditions, making it ideal for stepwise solid-phase or solution-phase peptide coupling. Commonly employed in the preparation of bioactive peptides related to neurodegenerative disease research, particularly those targeting dopamine receptors or melanin pathways. Also utilized in the development of enzyme inhibitors and diagnostic probes due to its structural similarity to natural catecholamine precursors. Stable under a range of reaction conditions, it supports multi-step syntheses in medicinal chemistry.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 50mg | 10-20 days | ฿24,420.00 |
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(2s)-2-[(benzyloxy)carbonyl]amino-3-(3,4-dihydroxyphenyl)propanoic acid
Widely used in peptide synthesis as a protected form of L-DOPA, enabling the controlled assembly of complex peptides without unwanted side reactions at the catechol group. The benzyloxycarbonyl (Cbz) protecting group allows for selective deprotection under mild conditions, making it ideal for stepwise solid-phase or solution-phase peptide coupling. Commonly employed in the preparation of bioactive peptides related to neurodegenerative disease research, particularly those targeting dopamine receptors or melanin pathways. Also utilized in the development of enzyme inhibitors and diagnostic probes due to its structural similarity to natural catecholamine precursors. Stable under a range of reaction conditions, it supports multi-step syntheses in medicinal chemistry.
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