(R)-1-(3-(Difluoromethyl)-2-fluorophenyl)ethan-1-amine hydrochloride
98%
- Product Code: 113448
CAS:
2569698-42-4
| Molecular Weight: | 225.64 g./mol | Molecular Formula: | C₉H₁₁ClF₃N |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD32671403 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8 ℃, inert gas storage |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of active pharmaceutical ingredients (APIs). It serves as a chiral building block in the creation of enantiomerically pure drugs, which are crucial for ensuring the efficacy and safety of medications. Its specific structure, featuring difluoromethyl and fluorine substituents, makes it valuable in the design of compounds targeting neurological and psychiatric disorders. Additionally, it is employed in the development of small molecule inhibitors for enzymes or receptors involved in disease pathways, contributing to advancements in precision medicine. Its hydrochloride form enhances solubility, facilitating its use in various formulations and experimental protocols.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,337.00 |
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| 0.250 | 10-20 days | ฿8,001.00 |
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(R)-1-(3-(Difluoromethyl)-2-fluorophenyl)ethan-1-amine hydrochloride
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of active pharmaceutical ingredients (APIs). It serves as a chiral building block in the creation of enantiomerically pure drugs, which are crucial for ensuring the efficacy and safety of medications. Its specific structure, featuring difluoromethyl and fluorine substituents, makes it valuable in the design of compounds targeting neurological and psychiatric disorders. Additionally, it is employed in the development of small molecule inhibitors for enzymes or receptors involved in disease pathways, contributing to advancements in precision medicine. Its hydrochloride form enhances solubility, facilitating its use in various formulations and experimental protocols.
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