6-Vinylpicolinaldehyde

98%

Reagent Code: #245517
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CAS Number 579500-16-6

science Other reagents with same CAS 579500-16-6

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Weight 133.15 g/mol
Formula C₈H₇NO
badge Registry Numbers
MDL Number MFCD18816459
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used in organic synthesis as a versatile building block for pharmaceuticals and agrochemicals, 6-Vinylpicolinaldehyde serves as a key intermediate in the preparation of nitrogen-containing heterocyclic compounds. Its aldehyde and vinyl functional groups allow for diverse reactions, including condensation, cyclization, and metal-catalyzed coupling, enabling the construction of complex molecular frameworks. It is particularly valuable in the development of catalysts and ligands for asymmetric synthesis. Additionally, it finds use in the research of fluorescent probes due to its ability to form conjugated systems upon derivatization.

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inventory 100mg
10-20 days ฿23,120.00

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6-Vinylpicolinaldehyde
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Used in organic synthesis as a versatile building block for pharmaceuticals and agrochemicals, 6-Vinylpicolinaldehyde serves as a key intermediate in the preparation of nitrogen-containing heterocyclic compounds. Its aldehyde and vinyl functional groups allow for diverse reactions, including condensation, cyclization, and metal-catalyzed coupling, enabling the construction of complex molecular frameworks. It is particularly valuable in the development of catalysts and ligands for asymmetric synthesis. Ad

Used in organic synthesis as a versatile building block for pharmaceuticals and agrochemicals, 6-Vinylpicolinaldehyde serves as a key intermediate in the preparation of nitrogen-containing heterocyclic compounds. Its aldehyde and vinyl functional groups allow for diverse reactions, including condensation, cyclization, and metal-catalyzed coupling, enabling the construction of complex molecular frameworks. It is particularly valuable in the development of catalysts and ligands for asymmetric synthesis. Additionally, it finds use in the research of fluorescent probes due to its ability to form conjugated systems upon derivatization.

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