N-Cbz-4-aminocyclohexanone
97%
- Product Code: 72776
Alias:
N-Cbz-p-Aminocyclohexanone
CAS:
16801-63-1
| Molecular Weight: | 247.29 g./mol | Molecular Formula: | C₁₄H₁₇NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06658393 | |
| Melting Point: | 86-87°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
N-Cbz-4-aminocyclohexanone is widely used in organic synthesis as a key intermediate in the preparation of various pharmaceuticals and bioactive compounds. Its protected amine group (Cbz) allows for selective reactions, making it valuable in the synthesis of complex molecules. It is particularly useful in the development of drugs targeting neurological disorders and cancer, where cyclohexane-based structures are often required. Additionally, it serves as a building block in the production of peptidomimetics and other drug-like molecules, enabling the exploration of structure-activity relationships in medicinal chemistry. Its versatility also extends to the synthesis of chiral compounds, aiding in the creation of enantiomerically pure substances.
Product Specification:
| Test | Specification |
|---|---|
| ELEMENTAL ANALYSISC | 65.6-70.4 |
| NITROGEN | 5.5 5.9% |
| PurityGC | 97 100% |
| APPEARANCE | White to tan powder,crystals and/or chunks |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $25.50 |
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| 5.000 | 10-20 days | $84.01 |
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| 25.000 | 10-20 days | $340.53 |
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N-Cbz-4-aminocyclohexanone
N-Cbz-4-aminocyclohexanone is widely used in organic synthesis as a key intermediate in the preparation of various pharmaceuticals and bioactive compounds. Its protected amine group (Cbz) allows for selective reactions, making it valuable in the synthesis of complex molecules. It is particularly useful in the development of drugs targeting neurological disorders and cancer, where cyclohexane-based structures are often required. Additionally, it serves as a building block in the production of peptidomimetics and other drug-like molecules, enabling the exploration of structure-activity relationships in medicinal chemistry. Its versatility also extends to the synthesis of chiral compounds, aiding in the creation of enantiomerically pure substances.
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