(R)-2-Amino-2-(3-bromo-4-chlorophenyl)ethan-1-ol hydrochloride

98%

Reagent Code: #229333
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CAS Number 2703746-09-0

science Other reagents with same CAS 2703746-09-0

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scatter_plot Molecular Information
Weight 286.98 g/mol
Formula C₈H₁₀BrCl₂NO
badge Registry Numbers
MDL Number MFCD24428637
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of serotonin and norepinephrine reuptake inhibitors (SNRIs). Its stereochemistry enables selective biological activity, making it valuable in producing antidepressants and anxiolytic drugs. The compound’s structure allows for effective binding to neurotransmitter transporters, enhancing its pharmacological relevance. It is also employed in the preparation of β-adrenergic receptor modulators due to its affinity for adrenergic pathways. Commonly utilized in asymmetric synthesis routes to ensure high enantiomeric purity in active pharmaceutical ingredients (APIs).

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿20,270.00
inventory 250mg
10-20 days ฿30,350.00

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(R)-2-Amino-2-(3-bromo-4-chlorophenyl)ethan-1-ol hydrochloride
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Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of serotonin and norepinephrine reuptake inhibitors (SNRIs). Its stereochemistry enables selective biological activity, making it valuable in producing antidepressants and anxiolytic drugs. The compound’s structure allows for effective binding to neurotransmitter transporters, enhancing its pharmacological relevance. It is also employed in the preparation of β-adrenergic receptor modulators due to

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of serotonin and norepinephrine reuptake inhibitors (SNRIs). Its stereochemistry enables selective biological activity, making it valuable in producing antidepressants and anxiolytic drugs. The compound’s structure allows for effective binding to neurotransmitter transporters, enhancing its pharmacological relevance. It is also employed in the preparation of β-adrenergic receptor modulators due to its affinity for adrenergic pathways. Commonly utilized in asymmetric synthesis routes to ensure high enantiomeric purity in active pharmaceutical ingredients (APIs).

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