(R)-7-Chloro-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride

98%

Reagent Code: #228625
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CAS Number 1257526-91-2

science Other reagents with same CAS 1257526-91-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.12 g/mol
Formula C₁₀H₁₃Cl₂N
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 development 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 products. Commonly employed in asymmetric synthesis routes where the (R)-configuration enhances binding affinity to specific neurotransmitter targets. Also utilized in research settings for developing novel analogs in medicinal chemistry programs focused on antidepressants and anxiolytics.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿18,870.00
inventory 250mg
10-20 days ฿32,050.00
inventory 1g
10-20 days ฿86,500.00

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(R)-7-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 development 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 products. Commonly employed in asymmetric synthesis routes where the (R)-configuration enhances binding affinity to specific neurotransmitter targets. Also utilized in rese

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development 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 products. Commonly employed in asymmetric synthesis routes where the (R)-configuration enhances binding affinity to specific neurotransmitter targets. Also utilized in research settings for developing novel analogs in medicinal chemistry programs focused on antidepressants and anxiolytics.

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