N-(5,6-diethyl-2,3-dihydro-1H-inden-2-yl)-2,2,2-trifluoro-Acetamide

98%

Reagent Code: #214785
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CAS Number 601487-90-5

science Other reagents with same CAS 601487-90-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 285.30 g/mol
Formula C₁₅H₁₈F₃NO
badge Registry Numbers
MDL Number MFCD28400028
thermostat Physical Properties
Melting Point 155-156 °C
Boiling Point 364.7±42.0 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.19±0.1 g/cm3(Predicted)
Storage Room temperature, sealed

description Product Description

Used in pharmaceutical research as an intermediate in the synthesis of dopamine receptor modulators. Its structure supports binding affinity to CNS targets, making it valuable in developing treatments for neurological disorders such as Parkinson’s disease and schizophrenia. The trifluoroacetamide group enhances metabolic stability, while the diethylindenyl moiety contributes to lipophilicity and blood-brain barrier penetration. Commonly employed in structure-activity relationship (SAR) studies to optimize potency and selectivity in dopaminergic compounds.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100g
10-20 days ฿77,000.00
N-(5,6-diethyl-2,3-dihydro-1H-inden-2-yl)-2,2,2-trifluoro-Acetamide
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Used in pharmaceutical research as an intermediate in the synthesis of dopamine receptor modulators. Its structure supports binding affinity to CNS targets, making it valuable in developing treatments for neurological disorders such as Parkinson’s disease and schizophrenia. The trifluoroacetamide group enhances metabolic stability, while the diethylindenyl moiety contributes to lipophilicity and blood-brain barrier penetration. Commonly employed in structure-activity relationship (SAR) studies to optimiz

Used in pharmaceutical research as an intermediate in the synthesis of dopamine receptor modulators. Its structure supports binding affinity to CNS targets, making it valuable in developing treatments for neurological disorders such as Parkinson’s disease and schizophrenia. The trifluoroacetamide group enhances metabolic stability, while the diethylindenyl moiety contributes to lipophilicity and blood-brain barrier penetration. Commonly employed in structure-activity relationship (SAR) studies to optimize potency and selectivity in dopaminergic compounds.

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