N-[4-Cyano-3-(trifluoromethyl)phenyl]-3-[(4-fluorophenyl)thio]-2-hydroxy-2-methylpropionamide

≥98%

Reagent Code: #217483
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CAS Number 90356-78-8

science Other reagents with same CAS 90356-78-8

blur_circular Chemical Specifications

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Weight 398.37 g/mol
Formula C₁₈H₁₄F₄N₂O₂S
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of Janus kinase (JAK) inhibitors, particularly in the development of pharmaceuticals targeting inflammatory and autoimmune diseases such as rheumatoid arthritis, psoriasis, and myelofibrosis. Its structure enables selective modulation of JAK enzyme activity, contributing to reduced cytokine signaling. It is employed in research and development for oral therapeutics due to its favorable binding properties and metabolic stability. Also utilized in structure-activity relationship (SAR) studies to optimize potency and selectivity in drug candidates.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,180.00
inventory 25g
10-20 days ฿8,720.00
inventory 100g
10-20 days ฿25,890.00
inventory 5g
10-20 days ฿2,730.00

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N-[4-Cyano-3-(trifluoromethyl)phenyl]-3-[(4-fluorophenyl)thio]-2-hydroxy-2-methylpropionamide
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Used as a key intermediate in the synthesis of Janus kinase (JAK) inhibitors, particularly in the development of pharmaceuticals targeting inflammatory and autoimmune diseases such as rheumatoid arthritis, psoriasis, and myelofibrosis. Its structure enables selective modulation of JAK enzyme activity, contributing to reduced cytokine signaling. It is employed in research and development for oral therapeutics due to its favorable binding properties and metabolic stability. Also utilized in structure-activ

Used as a key intermediate in the synthesis of Janus kinase (JAK) inhibitors, particularly in the development of pharmaceuticals targeting inflammatory and autoimmune diseases such as rheumatoid arthritis, psoriasis, and myelofibrosis. Its structure enables selective modulation of JAK enzyme activity, contributing to reduced cytokine signaling. It is employed in research and development for oral therapeutics due to its favorable binding properties and metabolic stability. Also utilized in structure-activity relationship (SAR) studies to optimize potency and selectivity in drug candidates.

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