8-Amino-1-(trifluoromethyl)-1,2,3,5,6,7-hexahydro-s-indacen-1-ol

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Reagent Code: #233327
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CAS Number 2676863-22-0

science Other reagents with same CAS 2676863-22-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.25 g/mol
Formula C₁₃H₁₄F₃NO
thermostat Physical Properties
Boiling Point 353.0±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.442±0.06 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of selective serotonin reuptake inhibitors (SSRIs), particularly in the production of antidepressant pharmaceuticals. Its unique trifluoromethyl and amino-hydroxy functionality enables enhanced binding affinity to neurotransmitter transporters, improving the potency and metabolic stability of the final drug compound. It is also employed in the development of neuroimaging agents due to its ability to cross the blood-brain barrier efficiently. Additionally, this compound serves as a building block in medicinal chemistry for designing novel CNS-active agents with optimized pharmacokinetic profiles.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,150.00
inventory 250mg
10-20 days ฿8,580.00

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8-Amino-1-(trifluoromethyl)-1,2,3,5,6,7-hexahydro-s-indacen-1-ol
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Used as a key intermediate in the synthesis of selective serotonin reuptake inhibitors (SSRIs), particularly in the production of antidepressant pharmaceuticals. Its unique trifluoromethyl and amino-hydroxy functionality enables enhanced binding affinity to neurotransmitter transporters, improving the potency and metabolic stability of the final drug compound. It is also employed in the development of neuroimaging agents due to its ability to cross the blood-brain barrier efficiently. Additionally, this com
Used as a key intermediate in the synthesis of selective serotonin reuptake inhibitors (SSRIs), particularly in the production of antidepressant pharmaceuticals. Its unique trifluoromethyl and amino-hydroxy functionality enables enhanced binding affinity to neurotransmitter transporters, improving the potency and metabolic stability of the final drug compound. It is also employed in the development of neuroimaging agents due to its ability to cross the blood-brain barrier efficiently. Additionally, this compound serves as a building block in medicinal chemistry for designing novel CNS-active agents with optimized pharmacokinetic profiles.
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