N-Allyl-4,5-dimethyl-2-(trimethylsilyl)thiophene-3-carboxamide

≥98%

Reagent Code: #218462
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CAS Number 175217-20-6

science Other reagents with same CAS 175217-20-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 267.46 g/mol
Formula C₁₃H₂₁NOSSi
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MDL Number MFCD04112621
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of bioactive molecules with insecticidal or fungicidal properties. Its structural features, including the thiophene ring and silyl group, enhance stability and reactivity in cross-coupling reactions, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Also employed in research settings to design novel organic semiconductors and functional materials due to its electron-rich character and potential for π-conjugation.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿15,500.00

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N-Allyl-4,5-dimethyl-2-(trimethylsilyl)thiophene-3-carboxamide
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Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of bioactive molecules with insecticidal or fungicidal properties. Its structural features, including the thiophene ring and silyl group, enhance stability and reactivity in cross-coupling reactions, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Also employed in research settings to design novel organic semiconductors and functional materials due to its
Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of bioactive molecules with insecticidal or fungicidal properties. Its structural features, including the thiophene ring and silyl group, enhance stability and reactivity in cross-coupling reactions, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Also employed in research settings to design novel organic semiconductors and functional materials due to its electron-rich character and potential for π-conjugation.
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