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

95%

Reagent Code: #233484
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CAS Number 2703745-64-4

science Other reagents with same CAS 2703745-64-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 286.98 g/mol
Formula C₈H₁₀BrCl₂NO
badge Registry Numbers
MDL Number MFCD24417117
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. Its stereochemistry allows for high enantioselectivity in drug synthesis, improving efficacy and reducing side effects. Commonly employed in the development of antidepressants and anxiolytic drugs due to its ability to influence neurotransmitter pathways. Also utilized in research settings for asymmetric synthesis and development of novel bioactive molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿22,050.00
inventory 250mg
10-20 days ฿33,020.00
(S)-2-Amino-2-(4-bromo-2-chlorophenyl)ethan-1-ol hydrochloride
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. Its stereochemistry allows for high enantioselectivity in drug synthesis, improving efficacy and reducing side effects. Commonly employed in the development of antidepressants and anxiolytic drugs due to its ability to influence neurotransmitter pathways. Also utilized in research settings for asymmetric synthesis

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. Its stereochemistry allows for high enantioselectivity in drug synthesis, improving efficacy and reducing side effects. Commonly employed in the development of antidepressants and anxiolytic drugs due to its ability to influence neurotransmitter pathways. Also utilized in research settings for asymmetric synthesis and development of novel bioactive molecules.

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