3-Cyclohexene-1-carboxylic acid, (1S)-, compd. with (αR)-α-methylbenzenemethanamine (1:1)
Chiral pure 99%
- Product Code: 44660
CAS:
67976-82-3
| Molecular Weight: | 247.33274 g./mol | Molecular Formula: | C₁₅H₂₁NO₂ |
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| Density: | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of chiral intermediates. Its structure, featuring a cyclohexene ring and a carboxylic acid group, makes it valuable for creating enantiomerically pure compounds, which are crucial in the production of active pharmaceutical ingredients (APIs). The presence of (αR)-α-methylbenzenemethanamine enhances its role in asymmetric synthesis, enabling the formation of specific stereoisomers with high selectivity. This is especially important in the design of drugs where the biological activity is highly dependent on the stereochemistry of the molecule. Additionally, it may be employed in organic synthesis for constructing complex molecules with defined spatial arrangements, contributing to advancements in medicinal chemistry and drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 25.000 | 10-20 days | €125.37 |
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| 100.000 | 10-20 days | €372.30 |
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3-Cyclohexene-1-carboxylic acid, (1S)-, compd. with (αR)-α-methylbenzenemethanamine (1:1)
This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of chiral intermediates. Its structure, featuring a cyclohexene ring and a carboxylic acid group, makes it valuable for creating enantiomerically pure compounds, which are crucial in the production of active pharmaceutical ingredients (APIs). The presence of (αR)-α-methylbenzenemethanamine enhances its role in asymmetric synthesis, enabling the formation of specific stereoisomers with high selectivity. This is especially important in the design of drugs where the biological activity is highly dependent on the stereochemistry of the molecule. Additionally, it may be employed in organic synthesis for constructing complex molecules with defined spatial arrangements, contributing to advancements in medicinal chemistry and drug discovery.
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