1-Boc-2-methyl-DL-proline
98%
- Product Code: 104411
CAS:
203869-80-1
| Molecular Weight: | 229.27 g./mol | Molecular Formula: | C₁₁H₁₉NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03095494 | |
| Melting Point: | Boiling Point: | 337.8°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
1-Boc-2-methyl-DL-proline is widely used in organic synthesis, particularly in the preparation of peptides and peptidomimetics. Its Boc (tert-butyloxycarbonyl) protecting group is essential for safeguarding the amino group during complex chemical reactions, allowing selective deprotection when needed. This compound is a valuable intermediate in medicinal chemistry for designing and synthesizing drug candidates, especially those targeting enzymes or receptors where proline derivatives play a role. It is also employed in the development of chiral catalysts and ligands for asymmetric synthesis, enhancing stereochemical control in reactions. Additionally, it finds application in the study of peptide structure-activity relationships, aiding in the optimization of bioactive molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,709.00 |
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| 1.000 | 10-20 days | ฿5,526.00 |
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| 5.000 | 10-20 days | ฿13,770.00 |
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1-Boc-2-methyl-DL-proline
1-Boc-2-methyl-DL-proline is widely used in organic synthesis, particularly in the preparation of peptides and peptidomimetics. Its Boc (tert-butyloxycarbonyl) protecting group is essential for safeguarding the amino group during complex chemical reactions, allowing selective deprotection when needed. This compound is a valuable intermediate in medicinal chemistry for designing and synthesizing drug candidates, especially those targeting enzymes or receptors where proline derivatives play a role. It is also employed in the development of chiral catalysts and ligands for asymmetric synthesis, enhancing stereochemical control in reactions. Additionally, it finds application in the study of peptide structure-activity relationships, aiding in the optimization of bioactive molecules.
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