6-(2-(Methylsulfonyl)pyrimidin-5-yl)-N-(prop-2-yn-1-yl)hex-5-ynamide

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Reagent Code: #210184
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CAS Number 2288710-39-2

science Other reagents with same CAS 2288710-39-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 305.35 g/mol
Formula C₁₄H₁₅N₃O₃S
badge Registry Numbers
MDL Number MFCD31715256
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of targeted cancer therapies, particularly kinase inhibitors. Its alkyne and pyrimidine functional groups enable selective binding to enzyme active sites, making it valuable in developing drugs that modulate signaling pathways in tumor cells. Also employed in click chemistry reactions for bioconjugation and probe development due to the terminal alkyne moiety, allowing attachment to biomolecules for imaging or diagnostic applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,460.00
inventory 250mg
10-20 days ฿3,660.00
inventory 1g
10-20 days ฿9,120.00

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6-(2-(Methylsulfonyl)pyrimidin-5-yl)-N-(prop-2-yn-1-yl)hex-5-ynamide
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Used in pharmaceutical research as a key intermediate in the synthesis of targeted cancer therapies, particularly kinase inhibitors. Its alkyne and pyrimidine functional groups enable selective binding to enzyme active sites, making it valuable in developing drugs that modulate signaling pathways in tumor cells. Also employed in click chemistry reactions for bioconjugation and probe development due to the terminal alkyne moiety, allowing attachment to biomolecules for imaging or diagnostic applications.<

Used in pharmaceutical research as a key intermediate in the synthesis of targeted cancer therapies, particularly kinase inhibitors. Its alkyne and pyrimidine functional groups enable selective binding to enzyme active sites, making it valuable in developing drugs that modulate signaling pathways in tumor cells. Also employed in click chemistry reactions for bioconjugation and probe development due to the terminal alkyne moiety, allowing attachment to biomolecules for imaging or diagnostic applications.

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