(R)-1-(2,2-difluoro-benzo[1,3]dioxol-4-yl)-ethylamine
95%
- Product Code: 37306
CAS:
1213203-92-9
| Molecular Weight: | 201.17 g./mol | Molecular Formula: | C₉H₉F₂NO₂ |
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| EC Number: | MDL Number: | MFCD09829311 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as a chiral building block for the synthesis of various active pharmaceutical ingredients (APIs). Its unique structure, featuring a difluoro-benzo[1,3]dioxol moiety, makes it valuable in the development of drugs targeting neurological disorders, particularly those involving modulation of neurotransmitter systems. It is often employed in the creation of selective inhibitors or agonists for specific receptors, contributing to the treatment of conditions like depression, anxiety, and chronic pain. Additionally, its chiral nature allows for the production of enantiomerically pure compounds, enhancing the efficacy and reducing the side effects of the resulting drugs. The compound's stability and reactivity also make it a suitable intermediate in organic synthesis for complex molecular architectures.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $385.79 |
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(R)-1-(2,2-difluoro-benzo[1,3]dioxol-4-yl)-ethylamine
This compound is primarily utilized in the pharmaceutical industry as a chiral building block for the synthesis of various active pharmaceutical ingredients (APIs). Its unique structure, featuring a difluoro-benzo[1,3]dioxol moiety, makes it valuable in the development of drugs targeting neurological disorders, particularly those involving modulation of neurotransmitter systems. It is often employed in the creation of selective inhibitors or agonists for specific receptors, contributing to the treatment of conditions like depression, anxiety, and chronic pain. Additionally, its chiral nature allows for the production of enantiomerically pure compounds, enhancing the efficacy and reducing the side effects of the resulting drugs. The compound's stability and reactivity also make it a suitable intermediate in organic synthesis for complex molecular architectures.
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