(R)-2-Aminopent-4-ynoic acid hydrochloride
≥95%
- Product Code: 37776
CAS:
87205-47-8
| Molecular Weight: | 149.58 g./mol | Molecular Formula: | C₅H₈ClNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09263338 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
(R)-2-Aminopent-4-ynoic acid hydrochloride is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the production of various bioactive compounds, particularly those targeting neurological and metabolic disorders. Its unique structure, featuring both an amino group and an alkyne moiety, makes it valuable for click chemistry applications, enabling the formation of complex molecules through efficient and selective reactions. Additionally, it is employed in the development of peptide-based drugs and as a building block for designing enzyme inhibitors. Its role in medicinal chemistry is significant, contributing to the creation of novel therapeutics with potential applications in treating diseases such as cancer and neurodegenerative conditions.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white powder or crystals |
| PURITY | 95-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | £23.75 |
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| 1.000 | 10-20 days | £67.40 |
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| 5.000 | 10-20 days | £250.60 |
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(R)-2-Aminopent-4-ynoic acid hydrochloride
(R)-2-Aminopent-4-ynoic acid hydrochloride is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the production of various bioactive compounds, particularly those targeting neurological and metabolic disorders. Its unique structure, featuring both an amino group and an alkyne moiety, makes it valuable for click chemistry applications, enabling the formation of complex molecules through efficient and selective reactions. Additionally, it is employed in the development of peptide-based drugs and as a building block for designing enzyme inhibitors. Its role in medicinal chemistry is significant, contributing to the creation of novel therapeutics with potential applications in treating diseases such as cancer and neurodegenerative conditions.
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