(E)-5-(2,3-bis(tert-butoxycarbonyl)guanidino)pentanoic acid
95%
- Product Code: 86739
CAS:
212567-95-8
| Molecular Weight: | 359.42 g./mol | Molecular Formula: | C₁₆H₂₉N₃O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD26940326 | |
| Melting Point: | Boiling Point: | ||
| Density: | 1.15±0.1 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in the synthesis of peptides and peptidomimetics, particularly in the preparation of arginine analogs. It serves as a protected guanidino building block, enabling the introduction of guanidine functionality into peptide chains while preventing unwanted side reactions during synthesis. The tert-butoxycarbonyl (Boc) groups provide stability under various reaction conditions, making it a valuable intermediate in solid-phase peptide synthesis. Additionally, it is utilized in the development of biologically active compounds, such as enzyme inhibitors and receptor ligands, where the guanidine moiety plays a critical role in binding interactions. Its application extends to medicinal chemistry, where it aids in the design of drug candidates targeting diseases like cancer, cardiovascular disorders, and infectious diseases.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $611.15 |
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| 0.250 | 10-20 days | $1,008.04 |
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| 1.000 | 10-20 days | $1,645.40 |
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(E)-5-(2,3-bis(tert-butoxycarbonyl)guanidino)pentanoic acid
This chemical is primarily used in the synthesis of peptides and peptidomimetics, particularly in the preparation of arginine analogs. It serves as a protected guanidino building block, enabling the introduction of guanidine functionality into peptide chains while preventing unwanted side reactions during synthesis. The tert-butoxycarbonyl (Boc) groups provide stability under various reaction conditions, making it a valuable intermediate in solid-phase peptide synthesis. Additionally, it is utilized in the development of biologically active compounds, such as enzyme inhibitors and receptor ligands, where the guanidine moiety plays a critical role in binding interactions. Its application extends to medicinal chemistry, where it aids in the design of drug candidates targeting diseases like cancer, cardiovascular disorders, and infectious diseases.
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