phenyl(pyrimidin-2-yl)methanone

98%

Reagent Code: #227914
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CAS Number 112170-34-0

science Other reagents with same CAS 112170-34-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 184.19 g/mol
Formula C₁₁H₈N₂O
badge Registry Numbers
MDL Number MFCD12153432
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, making it valuable in designing drugs targeting protein kinases involved in tumor growth. Also applied in agrochemical research for developing novel pesticides due to its ability to enhance molecular stability and bioavailability. Commonly employed in medicinal chemistry for scaffold modification to improve pharmacokinetic properties of lead compounds.

Available Sizes & Pricing

Size Availability Unit Price Quantity
500mg
10-20 days ฿31,470.00
phenyl(pyrimidin-2-yl)methanone
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, making it valuable in designing drugs targeting protein kinases involved in tumor growth. Also applied in agrochemical research for developing novel pesticides due to its ability to enhance molecular stability and bioavailability. Commonly employed in medicinal chemistry for scaffold modification to impro

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, making it valuable in designing drugs targeting protein kinases involved in tumor growth. Also applied in agrochemical research for developing novel pesticides due to its ability to enhance molecular stability and bioavailability. Commonly employed in medicinal chemistry for scaffold modification to improve pharmacokinetic properties of lead compounds.

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