(S)-1-(2,3-Dihydrobenzo[b][1,4]dioxin-6-yl)ethan-1-amine

95%

Reagent Code: #236613
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CAS Number 1212163-78-4

science Other reagents with same CAS 1212163-78-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 179.22 g/mol
Formula C₁₀H₁₃NO₂
badge Registry Numbers
MDL Number MFCD06762018
inventory_2 Storage & Handling
Storage Room temperature, avoid light

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) active compounds. Its enantiomeric purity is critical for achieving desired biological activity and minimizing side effects in final drug formulations. Commonly employed in asymmetric synthesis routes where the (S)-configuration enhances binding affinity to neurotransmitter receptors. Also utilized in the development of agrochemicals and bioactive molecules requiring high stereochemical precision.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,960.00
inventory 250mg
10-20 days ฿11,780.00
inventory 1g
10-20 days ฿34,410.00

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(S)-1-(2,3-Dihydrobenzo[b][1,4]dioxin-6-yl)ethan-1-amine
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Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) active compounds. Its enantiomeric purity is critical for achieving desired biological activity and minimizing side effects in final drug formulations. Commonly employed in asymmetric synthesis routes where the (S)-configuration enhances binding affinity to neurotransmitter receptors. Also utilized in the deve

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) active compounds. Its enantiomeric purity is critical for achieving desired biological activity and minimizing side effects in final drug formulations. Commonly employed in asymmetric synthesis routes where the (S)-configuration enhances binding affinity to neurotransmitter receptors. Also utilized in the development of agrochemicals and bioactive molecules requiring high stereochemical precision.

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