1-(5-bromo-3-methylpyridin-2-yl)-2,2,2-trifluoroethan-1-one

95%

Reagent Code: #131539
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CAS Number 1448790-49-5

science Other reagents with same CAS 1448790-49-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 268.03 g/mol
Formula C₈H₅BrF₃NO
badge Registry Numbers
MDL Number MFCD27992315
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 selective binding to enzyme active sites, enhancing drug efficacy. Commonly employed in research settings for constructing pyridine-based bioactive molecules. Also utilized in agrochemical research for designing novel pesticides with improved environmental profiles. The compound's trifluoromethyl and bromo functional groups allow for further chemical modifications through cross-coupling reactions, making it valuable in medicinal chemistry and drug discovery pipelines.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,030.00
inventory 250mg
10-20 days ฿23,870.00

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1-(5-bromo-3-methylpyridin-2-yl)-2,2,2-trifluoroethan-1-one
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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 selective binding to enzyme active sites, enhancing drug efficacy. Commonly employed in research settings for constructing pyridine-based bioactive molecules. Also utilized in agrochemical research for designing novel pesticides with improved environmental profiles. The compound's trifluoromethyl and bromo functional groups allow

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 selective binding to enzyme active sites, enhancing drug efficacy. Commonly employed in research settings for constructing pyridine-based bioactive molecules. Also utilized in agrochemical research for designing novel pesticides with improved environmental profiles. The compound's trifluoromethyl and bromo functional groups allow for further chemical modifications through cross-coupling reactions, making it valuable in medicinal chemistry and drug discovery pipelines.

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