(S)-(-)-2-Amino-4-pentenoic acid hydrochloride
95%
- Product Code: 125109
Alias:
L-allylglycine
CAS:
195316-72-4
| Molecular Weight: | 151.59 g./mol | Molecular Formula: | C₅H₉NO₂HCl |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 283 °C (dec.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
(S)-(-)-2-Amino-4-pentenoic acid hydrochloride is primarily used in organic synthesis and pharmaceutical research. It serves as a chiral building block for the preparation of various biologically active compounds, including peptides and enzyme inhibitors. Its structure allows for the introduction of functional groups, making it valuable in the development of drugs targeting specific enzymes or receptors. Additionally, it is utilized in the study of amino acid metabolism and as a precursor in the synthesis of modified amino acids for biochemical research. Its chiral nature is particularly useful in asymmetric synthesis, enabling the production of enantiomerically pure compounds.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Light Yellow To Light Red Powder To Crystal |
| Purity (%) | 94.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | $33.22 |
+
-
|
| 1.000 | 10-20 days | $96.35 |
+
-
|
| 5.000 | 10-20 days | $343.44 |
+
-
|
(S)-(-)-2-Amino-4-pentenoic acid hydrochloride
(S)-(-)-2-Amino-4-pentenoic acid hydrochloride is primarily used in organic synthesis and pharmaceutical research. It serves as a chiral building block for the preparation of various biologically active compounds, including peptides and enzyme inhibitors. Its structure allows for the introduction of functional groups, making it valuable in the development of drugs targeting specific enzymes or receptors. Additionally, it is utilized in the study of amino acid metabolism and as a precursor in the synthesis of modified amino acids for biochemical research. Its chiral nature is particularly useful in asymmetric synthesis, enabling the production of enantiomerically pure compounds.
| Mechanism | - |
| Appearance | - |
| Longevity | - |
| Strength | - |
| Storage | - |
| Shelf Life | - |
| Allergen(s) | - |
| Dosage (Range) | - |
| Recommended Dosage | - |
| Dosage (Per Day) | - |
| Recommended Dosage (Per Day) | - |
| Mix Method | - |
| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
Cart
No products
Subtotal:
$0.00
$0.00
Total :