N-Benzyloxycarbonyl-D-alaninol
98%
- Product Code: 96208
Alias:
N-Benzyloxycarbonyl-D-aminopropanol
(R)-2-Cbz-Aminopropanol
CAS:
61425-27-2
| Molecular Weight: | 209.24 g./mol | Molecular Formula: | C₆H₅CH₂O₂CNHCHCH₃CH₂OH |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00672531 | |
| Melting Point: | 82-84°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
N-Benzyloxycarbonyl-D-alaninol is primarily used in organic synthesis, particularly in the preparation of peptides and peptidomimetics. It serves as a protected form of D-alaninol, allowing for selective reactions in complex synthetic pathways. This compound is valuable in the development of pharmaceuticals, especially in the design of enzyme inhibitors and receptor agonists/antagonists. Its protective group, benzyloxycarbonyl, can be easily removed under mild conditions, making it a versatile intermediate in multi-step synthesis. Additionally, it finds application in the study of stereochemistry and chiral synthesis, contributing to the production of optically active compounds.
Product Specification:
| Test | Specification |
|---|---|
| CARBON | 61.6 64.7% |
| NITROGEN | 6.5 6.9% |
| PURITY HPLC | 98 100% |
| A20DC2ETHANOL | 4.5-6.5 |
| APPEARANCE | WHITE POWDER OR CRYSTALS |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $39.68 |
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| 5.000 | 10-20 days | $164.24 |
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| 25.000 | 10-20 days | $638.87 |
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N-Benzyloxycarbonyl-D-alaninol
N-Benzyloxycarbonyl-D-alaninol is primarily used in organic synthesis, particularly in the preparation of peptides and peptidomimetics. It serves as a protected form of D-alaninol, allowing for selective reactions in complex synthetic pathways. This compound is valuable in the development of pharmaceuticals, especially in the design of enzyme inhibitors and receptor agonists/antagonists. Its protective group, benzyloxycarbonyl, can be easily removed under mild conditions, making it a versatile intermediate in multi-step synthesis. Additionally, it finds application in the study of stereochemistry and chiral synthesis, contributing to the production of optically active compounds.
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