7-Chloro-2-methyl-5-(trifluoromethyl)-1h-pyrrolo[3,2-b]pyridine-6-carbonitrile

98%

Reagent Code: #156679
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CAS Number 1268521-89-6

science Other reagents with same CAS 1268521-89-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 259.62 g/mol
Formula C₁₀H₅ClF₃N₃
badge Registry Numbers
MDL Number MFCD14706437
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

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 binding to specific enzyme active sites, enhancing selectivity and potency. Also employed in agrochemical research for designing novel pesticides with improved metabolic stability and mode of action. The presence of electron-withdrawing groups and hydrogen-bonding motifs makes it valuable in optimizing molecular properties during drug discovery.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,520.00
inventory 5g
10-20 days ฿8,800.00

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7-Chloro-2-methyl-5-(trifluoromethyl)-1h-pyrrolo[3,2-b]pyridine-6-carbonitrile
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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 binding to specific enzyme active sites, enhancing selectivity and potency. Also employed in agrochemical research for designing novel pesticides with improved metabolic stability and mode of action. The presence of electron-withdrawing groups and hydrogen-bonding motifs makes it valuable in optimizing molecular properties during

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 binding to specific enzyme active sites, enhancing selectivity and potency. Also employed in agrochemical research for designing novel pesticides with improved metabolic stability and mode of action. The presence of electron-withdrawing groups and hydrogen-bonding motifs makes it valuable in optimizing molecular properties during drug discovery.

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