(3S,5S)-3,5-Dimethylmorpholine hydrochloride
95%
- Product Code: 36791
CAS:
154634-94-3
| Molecular Weight: | 151.63 g./mol | Molecular Formula: | C₆H₁₄ClNO |
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| EC Number: | MDL Number: | MFCD16036180 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, inert gas |
Product Description:
(3S,5S)-3,5-Dimethylmorpholine hydrochloride is primarily used in organic synthesis as a chiral building block or intermediate. It is particularly valuable in the pharmaceutical industry for the development of enantiomerically pure compounds, which are crucial for producing drugs with specific biological activities. The compound’s stereochemistry allows it to be employed in asymmetric synthesis, aiding in the creation of complex molecules with high precision. Additionally, it can serve as a catalyst or ligand in various chemical reactions, enhancing the efficiency and selectivity of the process. Its application extends to research and development, where it is utilized to study stereochemical effects and optimize synthetic pathways for bioactive molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $191.05 |
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| 0.250 | 10-20 days | $330.53 |
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| 1.000 | 10-20 days | $1,107.41 |
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(3S,5S)-3,5-Dimethylmorpholine hydrochloride
(3S,5S)-3,5-Dimethylmorpholine hydrochloride is primarily used in organic synthesis as a chiral building block or intermediate. It is particularly valuable in the pharmaceutical industry for the development of enantiomerically pure compounds, which are crucial for producing drugs with specific biological activities. The compound’s stereochemistry allows it to be employed in asymmetric synthesis, aiding in the creation of complex molecules with high precision. Additionally, it can serve as a catalyst or ligand in various chemical reactions, enhancing the efficiency and selectivity of the process. Its application extends to research and development, where it is utilized to study stereochemical effects and optimize synthetic pathways for bioactive molecules.
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