trans-(N-Boc-4-aminocyclohexyl)acetic Acid
97%
- Product Code: 76619
CAS:
189153-10-4
| Molecular Weight: | 257.33 g./mol | Molecular Formula: | C₁₃H₂₃NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03844588 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is widely used in organic synthesis, particularly in the development of pharmaceuticals and bioactive molecules. Its structure, featuring a Boc-protected amine and a carboxylic acid group, makes it a versatile intermediate for the preparation of peptides, peptidomimetics, and other complex organic compounds. The Boc group provides stability during reactions, allowing selective deprotection when needed. It is often employed in the synthesis of drug candidates targeting various diseases, including cancer, inflammation, and neurological disorders. Additionally, its cyclohexyl ring contributes to conformational rigidity, which is beneficial in designing molecules with specific biological activities. This compound is also utilized in the production of chiral catalysts and ligands for asymmetric synthesis, enhancing the efficiency and selectivity of chemical transformations.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white Solid |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $23.60 |
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| 1.000 | 10-20 days | $71.18 |
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| 5.000 | 10-20 days | $270.96 |
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trans-(N-Boc-4-aminocyclohexyl)acetic Acid
This compound is widely used in organic synthesis, particularly in the development of pharmaceuticals and bioactive molecules. Its structure, featuring a Boc-protected amine and a carboxylic acid group, makes it a versatile intermediate for the preparation of peptides, peptidomimetics, and other complex organic compounds. The Boc group provides stability during reactions, allowing selective deprotection when needed. It is often employed in the synthesis of drug candidates targeting various diseases, including cancer, inflammation, and neurological disorders. Additionally, its cyclohexyl ring contributes to conformational rigidity, which is beneficial in designing molecules with specific biological activities. This compound is also utilized in the production of chiral catalysts and ligands for asymmetric synthesis, enhancing the efficiency and selectivity of chemical transformations.
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