8-(Trifluoromethyl)-1,2,3,4-tetrahydroisoquinoline

≥95%

Reagent Code: #238409
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CAS Number 284027-36-7

science Other reagents with same CAS 284027-36-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.1909 g/mol
Formula C₁₀H₁₀F₃N
badge Registry Numbers
MDL Number MFCD11223554
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) active agents. Its structure supports the design of compounds with dopaminergic and serotonergic activity, making it valuable in researching treatments for neurological disorders such as Parkinson’s disease and depression. The trifluoromethyl group enhances metabolic stability and bioavailability, which improves drug performance. It is also employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its rigid framework and ability to mimic bioactive conformations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,800.00
inventory 250mg
10-20 days ฿6,450.00
inventory 1g
10-20 days ฿17,410.00

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8-(Trifluoromethyl)-1,2,3,4-tetrahydroisoquinoline
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) active agents. Its structure supports the design of compounds with dopaminergic and serotonergic activity, making it valuable in researching treatments for neurological disorders such as Parkinson’s disease and depression. The trifluoromethyl group enhances metabolic stability and bioavailability, which improves drug performance. It is also employed in medicinal chemistry for st

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) active agents. Its structure supports the design of compounds with dopaminergic and serotonergic activity, making it valuable in researching treatments for neurological disorders such as Parkinson’s disease and depression. The trifluoromethyl group enhances metabolic stability and bioavailability, which improves drug performance. It is also employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its rigid framework and ability to mimic bioactive conformations.

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