L-Proline methyl ester hydrochloride
98%
- Product Code: 105344
Alias:
L-Proline methyl ester hydrochloride
CAS:
2133-40-6
| Molecular Weight: | 165.62 g./mol | Molecular Formula: | C₆H₁₂ClNO₂ |
|---|---|---|---|
| EC Number: | 218-363-0 | MDL Number: | MFCD00012708 |
| Melting Point: | 69-71 °C(lit.) | Boiling Point: | 55 °C / 11mmHg |
| Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
L-Proline methyl ester hydrochloride is widely used in organic synthesis, particularly in peptide chemistry. It serves as a building block for the preparation of proline-containing peptides and peptidomimetics, which are essential in drug discovery and development. The compound is also employed in asymmetric synthesis, where it acts as a chiral auxiliary to induce stereoselectivity in reactions, leading to the production of enantiomerically pure compounds. Additionally, it finds application in the synthesis of biologically active molecules, including inhibitors and ligands for various enzymes and receptors. Its stability and reactivity make it a valuable reagent in medicinal chemistry and biochemical research.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White Powder |
| Purity (%) | 97.5-100 |
| Melting Point | 70-80 |
| Specific Rotation [A]20/D(C=1, H2O) | -33 -30 |
| Infrared Spectrometry | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $14.95 |
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| 5.000 | 10-20 days | $23.26 |
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| 25.000 | 10-20 days | $33.22 |
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| 100.000 | 10-20 days | $104.65 |
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| 500.000 | 10-20 days | $509.98 |
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L-Proline methyl ester hydrochloride
L-Proline methyl ester hydrochloride is widely used in organic synthesis, particularly in peptide chemistry. It serves as a building block for the preparation of proline-containing peptides and peptidomimetics, which are essential in drug discovery and development. The compound is also employed in asymmetric synthesis, where it acts as a chiral auxiliary to induce stereoselectivity in reactions, leading to the production of enantiomerically pure compounds. Additionally, it finds application in the synthesis of biologically active molecules, including inhibitors and ligands for various enzymes and receptors. Its stability and reactivity make it a valuable reagent in medicinal chemistry and biochemical research.
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