(R)-1-(4-(Trifluoromethyl)phenyl)propan-1-amine hydrochloride

95%

Reagent Code: #37332
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CAS Number 856563-00-3

science Other reagents with same CAS 856563-00-3

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Weight 239.6651 g/mol
Formula C₁₀H₁₃ClF₃N
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MDL Number MFCD12757295
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description Product Description

This chiral compound, an (R)-enantiomer of 1-(4-(trifluoromethyl)phenyl)propan-1-amine hydrochloride, is utilized in pharmaceutical research and development, particularly for studying central nervous system effects. As an amphetamine derivative, it modulates monoamine neurotransmitters such as serotonin and dopamine, aiding investigations into psychoactive properties, mood disorders like depression and anxiety, and related psychiatric conditions. The trifluoromethyl group improves its metabolic stability, supporting pharmacokinetic studies. It is also employed in the synthesis of chiral intermediates for enantiomerically pure drug candidates.

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inventory 100mg
10-20 days ฿12,879.00

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(R)-1-(4-(Trifluoromethyl)phenyl)propan-1-amine hydrochloride
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This chiral compound, an (R)-enantiomer of 1-(4-(trifluoromethyl)phenyl)propan-1-amine hydrochloride, is utilized in pharmaceutical research and development, particularly for studying central nervous system effects. As an amphetamine derivative, it modulates monoamine neurotransmitters such as serotonin and dopamine, aiding investigations into psychoactive properties, mood disorders like depression and anxiety, and related psychiatric conditions. The trifluoromethyl group improves its metabolic stability

This chiral compound, an (R)-enantiomer of 1-(4-(trifluoromethyl)phenyl)propan-1-amine hydrochloride, is utilized in pharmaceutical research and development, particularly for studying central nervous system effects. As an amphetamine derivative, it modulates monoamine neurotransmitters such as serotonin and dopamine, aiding investigations into psychoactive properties, mood disorders like depression and anxiety, and related psychiatric conditions. The trifluoromethyl group improves its metabolic stability, supporting pharmacokinetic studies. It is also employed in the synthesis of chiral intermediates for enantiomerically pure drug candidates.

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