5-(trifluoromethyl)-N2,N2-dimethylpyridine-2,3-diamine

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Reagent Code: #216900
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CAS Number 874880-82-7

science Other reagents with same CAS 874880-82-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.18 g/mol
Formula C₈H₁₀F₃N₃
badge Registry Numbers
MDL Number MFCD08059434
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, enhancing selectivity and potency. Also employed in agrochemicals to improve metabolic stability and bioavailability. The trifluoromethyl group contributes to increased lipophilicity and resistance to oxidative degradation, making it valuable in designing long-acting compounds. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿22,520.00
inventory 250mg
10-20 days ฿38,270.00

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5-(trifluoromethyl)-N2,N2-dimethylpyridine-2,3-diamine
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, enhancing selectivity and potency. Also employed in agrochemicals to improve metabolic stability and bioavailability. The trifluoromethyl group contributes to increased lipophilicity and resistance to oxidative degradation, making it valuable in designing long-acting compounds. Commonly utilized in medicinal

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, enhancing selectivity and potency. Also employed in agrochemicals to improve metabolic stability and bioavailability. The trifluoromethyl group contributes to increased lipophilicity and resistance to oxidative degradation, making it valuable in designing long-acting compounds. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates.

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