2-(Imidazolidin-2-ylidene)-1-(p-tolyl)ethan-1-one

≥95%

Reagent Code: #201062
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CAS Number 82100-23-0

science Other reagents with same CAS 82100-23-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.25 g/mol
Formula C₁₂H₁₄N₂O
badge Registry Numbers
MDL Number MFCD18325088
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This specialty chemical serves as a stable N-heterocyclic carbene (NHC) catalyst in organic synthesis, particularly for transition metal-catalyzed cross-coupling reactions such as Heck and Fu-type couplings. It enhances C-C bond formation efficiency using metals like palladium, yielding high-purity products in pharmaceutical and advanced materials applications. Additionally, it functions as an intermediate for synthesizing biologically active compounds, including imidazoline-based drugs with potential antihypertensive or antimicrobial properties, and specialty heterocyclic compounds in medicinal chemistry research. Its conjugated structure supports advanced synthetic pathways for novel molecules with targeted bioactivity.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿46,680.00

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2-(Imidazolidin-2-ylidene)-1-(p-tolyl)ethan-1-one
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This specialty chemical serves as a stable N-heterocyclic carbene (NHC) catalyst in organic synthesis, particularly for transition metal-catalyzed cross-coupling reactions such as Heck and Fu-type couplings. It enhances C-C bond formation efficiency using metals like palladium, yielding high-purity products in pharmaceutical and advanced materials applications. Additionally, it functions as an intermediate for synthesizing biologically active compounds, including imidazoline-based drugs with potential an

This specialty chemical serves as a stable N-heterocyclic carbene (NHC) catalyst in organic synthesis, particularly for transition metal-catalyzed cross-coupling reactions such as Heck and Fu-type couplings. It enhances C-C bond formation efficiency using metals like palladium, yielding high-purity products in pharmaceutical and advanced materials applications. Additionally, it functions as an intermediate for synthesizing biologically active compounds, including imidazoline-based drugs with potential antihypertensive or antimicrobial properties, and specialty heterocyclic compounds in medicinal chemistry research. Its conjugated structure supports advanced synthetic pathways for novel molecules with targeted bioactivity.

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