(R)-1-(3-(Difluoromethyl)-2-fluorophenyl)ethan-1-amine hydrochloride

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Reagent Code: #113448
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CAS Number 2569698-42-4

science Other reagents with same CAS 2569698-42-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.64 g/mol
Formula C₉H₁₁ClF₃N
badge Registry Numbers
MDL Number MFCD32671403
inventory_2 Storage & Handling
Storage 2-8 ℃, inert gas storage

description 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.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿8,001.00
inventory 100mg
10-20 days ฿5,337.00

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(R)-1-(3-(Difluoromethyl)-2-fluorophenyl)ethan-1-amine hydrochloride
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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 employe

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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