(S)-2-aminohept-6-enoicacid
98%
- Product Code: 104140
CAS:
1666734-64-1
| Molecular Weight: | 143.2 g./mol | Molecular Formula: | C₇H₁₃NO₂ |
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| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
(S)-2-aminohept-6-enoic acid finds its application primarily in the field of organic synthesis and pharmaceutical research. It serves as a valuable building block for the development of complex molecules, particularly in the synthesis of peptides and amino acid derivatives. Its unique structure, featuring both an amino group and an alkene moiety, makes it a versatile intermediate for creating compounds with potential biological activity. Researchers utilize it in the design of drug candidates, especially those targeting enzymes or receptors where specific stereochemistry is crucial. Additionally, it can be employed in the study of metabolic pathways and the development of novel biomaterials. Its applications extend to the production of chiral compounds, where its enantiomeric purity is essential for achieving desired pharmacological effects.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿43,200.00 |
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(S)-2-aminohept-6-enoicacid
(S)-2-aminohept-6-enoic acid finds its application primarily in the field of organic synthesis and pharmaceutical research. It serves as a valuable building block for the development of complex molecules, particularly in the synthesis of peptides and amino acid derivatives. Its unique structure, featuring both an amino group and an alkene moiety, makes it a versatile intermediate for creating compounds with potential biological activity. Researchers utilize it in the design of drug candidates, especially those targeting enzymes or receptors where specific stereochemistry is crucial. Additionally, it can be employed in the study of metabolic pathways and the development of novel biomaterials. Its applications extend to the production of chiral compounds, where its enantiomeric purity is essential for achieving desired pharmacological effects.
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