(R)-5-Chloro-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride

95%

Reagent Code: #230847
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CAS Number 2055848-84-3

science Other reagents with same CAS 2055848-84-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.12 g/mol
Formula C₁₀H₁₃Cl₂N
badge Registry Numbers
MDL Number MFCD26586043
inventory_2 Storage & Handling
Storage Room temperature, inert gas

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 drugs. Its enantiomeric purity is critical for ensuring the desired pharmacological activity and minimizing side effects in final drug formulations. Commonly employed in asymmetric synthesis routes where the (R)-configuration contributes to higher binding affinity toward specific neurotransmitter receptors. Also utilized in the development of adrenergic and dopaminergic compounds for treating depression, anxiety, and neurodegenerative disorders.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿9,840.00

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(R)-5-Chloro-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride
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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 drugs. Its enantiomeric purity is critical for ensuring the desired pharmacological activity and minimizing side effects in final drug formulations. Commonly employed in asymmetric synthesis routes where the (R)-configuration contributes to higher binding affinity toward specific neurotransmitter recept

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 drugs. Its enantiomeric purity is critical for ensuring the desired pharmacological activity and minimizing side effects in final drug formulations. Commonly employed in asymmetric synthesis routes where the (R)-configuration contributes to higher binding affinity toward specific neurotransmitter receptors. Also utilized in the development of adrenergic and dopaminergic compounds for treating depression, anxiety, and neurodegenerative disorders.

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