2-Methyl-6-(trifluoromethyl)-1H-indole

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Reagent Code: #203347
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CAS Number 57330-48-0

science Other reagents with same CAS 57330-48-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.17 g/mol
Formula C₁₀H₈NF₃
badge Registry Numbers
MDL Number MFCD16875985
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. Its structure supports the design of bioactive molecules with enhanced metabolic stability due to the presence of the trifluoromethyl group. It also finds use in the preparation of kinase inhibitors and anti-inflammatory compounds. In research, it serves as a building block for novel indole-based derivatives in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,750.00
inventory 250mg
10-20 days ฿18,250.00
inventory 1g
10-20 days ฿49,250.00

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2-Methyl-6-(trifluoromethyl)-1H-indole
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Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. Its structure supports the design of bioactive molecules with enhanced metabolic stability due to the presence of the trifluoromethyl group. It also finds use in the preparation of kinase inhibitors and anti-inflammatory compounds. In research, it serves as a building block for novel indole-based derivatives in m

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. Its structure supports the design of bioactive molecules with enhanced metabolic stability due to the presence of the trifluoromethyl group. It also finds use in the preparation of kinase inhibitors and anti-inflammatory compounds. In research, it serves as a building block for novel indole-based derivatives in medicinal chemistry.

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