Ethyl 5-(trifluoromethyl)-1H-pyrrole-2-carboxylate

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Reagent Code: #184927
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CAS Number 1414887-27-6

science Other reagents with same CAS 1414887-27-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.15 g/mol
Formula C₈H₈F₃NO₂
badge Registry Numbers
MDL Number MFCD26516442
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds targeting central nervous system disorders and anti-inflammatory agents. Its structure supports the construction of complex heterocyclic systems, making it valuable in medicinal chemistry for drug discovery. The electron-withdrawing trifluoromethyl group enhances metabolic stability and binding affinity in final drug molecules. It is also employed in agrochemical research for designing novel pesticides and herbicides due to its favorable reactivity and structural properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,130.00
inventory 1g
10-20 days ฿33,200.00
inventory 250mg
10-20 days ฿9,490.00

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Ethyl 5-(trifluoromethyl)-1H-pyrrole-2-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds targeting central nervous system disorders and anti-inflammatory agents. Its structure supports the construction of complex heterocyclic systems, making it valuable in medicinal chemistry for drug discovery. The electron-withdrawing trifluoromethyl group enhances metabolic stability and binding affinity in final drug molecules. It is also employed in agrochemical research for d

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds targeting central nervous system disorders and anti-inflammatory agents. Its structure supports the construction of complex heterocyclic systems, making it valuable in medicinal chemistry for drug discovery. The electron-withdrawing trifluoromethyl group enhances metabolic stability and binding affinity in final drug molecules. It is also employed in agrochemical research for designing novel pesticides and herbicides due to its favorable reactivity and structural properties.

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