(R)-Methyl 5-(6-((4-Methylpiperazin-1-Yl)Methyl)-1H-Benzo[D]Imidazol-1-Yl)-3-(1-(2-(Trifluoromethyl)Phenyl)Ethoxy)Thiophene-2-Carboxylate

98%

Reagent Code: #231584
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CAS Number 929095-51-2

science Other reagents with same CAS 929095-51-2

blur_circular Chemical Specifications

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Weight 558.62 g/mol
Formula C₂₈H₂₉F₃N₄O₃S
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of selective kinase inhibitors, particularly targeting enzymes involved in inflammatory and oncogenic pathways. Its structural features enable strong binding to specific protein targets, making it valuable in developing treatments for cancer and autoimmune diseases. The compound's chirality enhances selectivity, reducing off-target effects in drug candidates. It is also employed in structure-activity relationship (SAR) studies to optimize potency and pharmacokinetic properties of new therapeutic agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿38,290.00
inventory 250mg
10-20 days ฿63,820.00

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(R)-Methyl 5-(6-((4-Methylpiperazin-1-Yl)Methyl)-1H-Benzo[D]Imidazol-1-Yl)-3-(1-(2-(Trifluoromethyl)Phenyl)Ethoxy)Thiophene-2-Carboxylate
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Used in pharmaceutical research as a key intermediate in the synthesis of selective kinase inhibitors, particularly targeting enzymes involved in inflammatory and oncogenic pathways. Its structural features enable strong binding to specific protein targets, making it valuable in developing treatments for cancer and autoimmune diseases. The compound's chirality enhances selectivity, reducing off-target effects in drug candidates. It is also employed in structure-activity relationship (SAR) studies to opti

Used in pharmaceutical research as a key intermediate in the synthesis of selective kinase inhibitors, particularly targeting enzymes involved in inflammatory and oncogenic pathways. Its structural features enable strong binding to specific protein targets, making it valuable in developing treatments for cancer and autoimmune diseases. The compound's chirality enhances selectivity, reducing off-target effects in drug candidates. It is also employed in structure-activity relationship (SAR) studies to optimize potency and pharmacokinetic properties of new therapeutic agents.

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