Dimethyl 3-(trifluoromethyl)pyridine-2,5-dicarboxylate

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Reagent Code: #177460
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CAS Number 1360944-09-7

science Other reagents with same CAS 1360944-09-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 263.17 g/mol
Formula C₁₀H₈F₃NO₄
badge Registry Numbers
MDL Number MFCD31652783
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 kinase inhibitors and other bioactive molecules. Its structure allows for further functionalization, making it valuable in medicinal chemistry for creating analogs with potential anti-inflammatory, anticancer, or antiviral activity. Also employed in agrochemical research for designing new crop protection agents due to the stability and electronic properties provided by the trifluoromethyl and pyridine groups. Commonly utilized in organic synthesis to build complex heterocyclic systems through transformations such as hydrolysis, reduction, or cross-coupling reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,440.00
inventory 250mg
10-20 days ฿5,940.00
inventory 1g
10-20 days ฿14,810.00

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Dimethyl 3-(trifluoromethyl)pyridine-2,5-dicarboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for further functionalization, making it valuable in medicinal chemistry for creating analogs with potential anti-inflammatory, anticancer, or antiviral activity. Also employed in agrochemical research for designing new crop protection agents due to the stability and electronic properties provided by the trifluoromethyl and pyridine group

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for further functionalization, making it valuable in medicinal chemistry for creating analogs with potential anti-inflammatory, anticancer, or antiviral activity. Also employed in agrochemical research for designing new crop protection agents due to the stability and electronic properties provided by the trifluoromethyl and pyridine groups. Commonly utilized in organic synthesis to build complex heterocyclic systems through transformations such as hydrolysis, reduction, or cross-coupling reactions.

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