1-((Isocyano(4-(trifluoromethyl)phenyl)methyl)sulfonyl)-4-methylbenzene

≥95%

Reagent Code: #201243
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CAS Number 748187-71-5

science Other reagents with same CAS 748187-71-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 339.33 g/mol
Formula C₁₆H₁₂F₃NO₂S
badge Registry Numbers
MDL Number MFCD04114778
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. Its isocyanide functional group enables participation in multicomponent reactions, such as the Ugi and Passerini reactions, which are valuable for constructing complex molecules with high atom efficiency. The presence of the sulfonyl and trifluoromethyl groups enhances reactivity and influences lipophilicity, making it useful in the design of bioactive compounds. It is also employed in medicinal chemistry research for scaffold diversification and library synthesis in drug discovery programs.

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inventory 1g
10-20 days ฿16,580.00

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1-((Isocyano(4-(trifluoromethyl)phenyl)methyl)sulfonyl)-4-methylbenzene
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Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. Its isocyanide functional group enables participation in multicomponent reactions, such as the Ugi and Passerini reactions, which are valuable for constructing complex molecules with high atom efficiency. The presence of the sulfonyl and trifluoromethyl groups enhances reactivity and influences lipophilicity, making it useful in the design of bioactive compounds. It is also employed

Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. Its isocyanide functional group enables participation in multicomponent reactions, such as the Ugi and Passerini reactions, which are valuable for constructing complex molecules with high atom efficiency. The presence of the sulfonyl and trifluoromethyl groups enhances reactivity and influences lipophilicity, making it useful in the design of bioactive compounds. It is also employed in medicinal chemistry research for scaffold diversification and library synthesis in drug discovery programs.

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