(S)-benzyl 2-((S)-2-(((benzyloxy)carbonyl)amino)-5-ureidopentanamido)-4-methylpentanoate
95%
- Product Code: 83019
CAS:
122411-98-7
| Molecular Weight: | 512.60 g./mol | Molecular Formula: | C₂₇H₃₆N₄O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD31803913 | |
| Melting Point: | 135-138 °C | Boiling Point: | 721.8±60.0 °C(Predicted) |
| Density: | 1.192±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in peptide synthesis and organic chemistry research. It serves as a key intermediate in the preparation of complex peptides, particularly those involving ureido functional groups. Its structure allows for selective deprotection and coupling reactions, making it valuable in the stepwise assembly of peptide chains. Additionally, it is used in the study of enzyme inhibitors and bioactive peptides, contributing to the development of pharmaceutical compounds. Its benzyl ester and carbamate protecting groups provide stability during synthesis, enabling precise control over reaction conditions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $1,318.75 |
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| 0.250 | 10-20 days | $2,307.81 |
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(S)-benzyl 2-((S)-2-(((benzyloxy)carbonyl)amino)-5-ureidopentanamido)-4-methylpentanoate
This compound is primarily utilized in peptide synthesis and organic chemistry research. It serves as a key intermediate in the preparation of complex peptides, particularly those involving ureido functional groups. Its structure allows for selective deprotection and coupling reactions, making it valuable in the stepwise assembly of peptide chains. Additionally, it is used in the study of enzyme inhibitors and bioactive peptides, contributing to the development of pharmaceutical compounds. Its benzyl ester and carbamate protecting groups provide stability during synthesis, enabling precise control over reaction conditions.
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