2-(Ethylsulfonyl)-4-(3-methoxyphenyl)-6-(trifluoromethyl)pyrimidine

97%

Reagent Code: #184903
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CAS Number 862785-73-7

science Other reagents with same CAS 862785-73-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 346.32 g/mol
Formula C₁₄H₁₃F₃N₂O₃S
badge Registry Numbers
MDL Number MFCD05861685
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure supports high binding affinity to specific enzyme active sites, making it valuable in drug discovery. Also employed in agrochemical research for designing novel pesticides with improved selectivity and environmental safety. The compound's stability and reactivity profile allow for efficient derivatization in multi-step organic syntheses.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,640.00
inventory 250mg
10-20 days ฿9,210.00

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2-(Ethylsulfonyl)-4-(3-methoxyphenyl)-6-(trifluoromethyl)pyrimidine
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure supports high binding affinity to specific enzyme active sites, making it valuable in drug discovery. Also employed in agrochemical research for designing novel pesticides with improved selectivity and environmental safety. The compound's stability and reactivity profile allow for efficient derivatization in multi-step organic syntheses.

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure supports high binding affinity to specific enzyme active sites, making it valuable in drug discovery. Also employed in agrochemical research for designing novel pesticides with improved selectivity and environmental safety. The compound's stability and reactivity profile allow for efficient derivatization in multi-step organic syntheses.

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