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

98%

Reagent Code: #231582
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CAS Number 929095-39-6

science Other reagents with same CAS 929095-39-6

blur_circular Chemical Specifications

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Weight 476.47 g/mol
Formula C₂₃H₁₉F₃N₂O₄S
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of selective enzyme inhibitors, particularly in the development of drugs targeting inflammatory and autoimmune diseases. Its structure supports high binding affinity to specific protein targets, making it valuable in optimizing pharmacokinetic properties of candidate molecules. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its chiral center and functional group versatility.

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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-(Hydroxymethyl)-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 enzyme inhibitors, particularly in the development of drugs targeting inflammatory and autoimmune diseases. Its structure supports high binding affinity to specific protein targets, making it valuable in optimizing pharmacokinetic properties of candidate molecules. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its chiral center and functional group versatility.

Used in pharmaceutical research as a key intermediate in the synthesis of selective enzyme inhibitors, particularly in the development of drugs targeting inflammatory and autoimmune diseases. Its structure supports high binding affinity to specific protein targets, making it valuable in optimizing pharmacokinetic properties of candidate molecules. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its chiral center and functional group versatility.

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