(R)-1-(3,4-Difluorophenyl)propan-1-amine hydrochloride

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Reagent Code: #231057
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CAS Number 1565825-89-9

science Other reagents with same CAS 1565825-89-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.651 g/mol
Formula C₉H₁₂ClF₂N
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) active agents. Its enantiomeric purity makes it valuable for creating selective serotonin reuptake inhibitors (SSRIs) and other neuropsychiatric drugs. The compound's fluorinated aromatic structure enhances blood-brain barrier penetration, improving efficacy in neuroactive compounds. It is also employed in the preparation of kinase inhibitors and anti-inflammatory agents due to its favorable binding properties with biological targets.

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inventory 1g
10-20 days ฿38,510.00

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(R)-1-(3,4-Difluorophenyl)propan-1-amine hydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) active agents. Its enantiomeric purity makes it valuable for creating selective serotonin reuptake inhibitors (SSRIs) and other neuropsychiatric drugs. The compound's fluorinated aromatic structure enhances blood-brain barrier penetration, improving efficacy in neuroactive compounds. It is also employed in the preparation of kinase inhibitors and anti-inflammatory agents du

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) active agents. Its enantiomeric purity makes it valuable for creating selective serotonin reuptake inhibitors (SSRIs) and other neuropsychiatric drugs. The compound's fluorinated aromatic structure enhances blood-brain barrier penetration, improving efficacy in neuroactive compounds. It is also employed in the preparation of kinase inhibitors and anti-inflammatory agents due to its favorable binding properties with biological targets.

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