tert-Butyl ((1S,2S)-2-((3-chlorobenzyl)oxy)cyclohexyl)carbamate
≥97%
- Product Code: 87831
CAS:
1956370-85-6
| Molecular Weight: | 339.86 g./mol | Molecular Formula: | C₁₈H₂₆ClNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD29059425 | |
| Melting Point: | Boiling Point: | 445.8±40.0 °C(Predicted) | |
| Density: | 1.14±0.1 g/cm3(Predicted) | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a key intermediate in the synthesis of complex molecules, often those with potential therapeutic applications. The presence of the tert-butyl carbamate group makes it a valuable protecting group for amines, ensuring stability during multi-step synthetic processes. Additionally, the 3-chlorobenzyl moiety can contribute to the biological activity of the final compound, making it relevant in drug discovery and medicinal chemistry. Its stereochemistry (1S,2S) is also crucial for creating enantiomerically pure substances, which is essential in the production of drugs with specific biological targets. Overall, it plays a significant role in the synthesis of bioactive molecules and drug candidates.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $118.88 |
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| 0.250 | 10-20 days | $279.36 |
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| 1.000 | 10-20 days | $1,077.20 |
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tert-Butyl ((1S,2S)-2-((3-chlorobenzyl)oxy)cyclohexyl)carbamate
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a key intermediate in the synthesis of complex molecules, often those with potential therapeutic applications. The presence of the tert-butyl carbamate group makes it a valuable protecting group for amines, ensuring stability during multi-step synthetic processes. Additionally, the 3-chlorobenzyl moiety can contribute to the biological activity of the final compound, making it relevant in drug discovery and medicinal chemistry. Its stereochemistry (1S,2S) is also crucial for creating enantiomerically pure substances, which is essential in the production of drugs with specific biological targets. Overall, it plays a significant role in the synthesis of bioactive molecules and drug candidates.
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