6-(Piperidin-1-yl)pyridine-3-carbaldehyde

≥95%

Reagent Code: #228195
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CAS Number 241816-11-5

science Other reagents with same CAS 241816-11-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.24 g/mol
Formula C₁₁H₁₄N₂O
badge Registry Numbers
MDL Number MFCD04117814
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for creating compounds with potential anticancer, anti-inflammatory, and neuroprotective activities. Commonly employed in the preparation of nitrogen-containing heterocyclic systems through condensation or coupling reactions. Also utilized in agrochemical research for designing new active ingredients. Its aldehyde group enables Schiff base formation, useful in coordination chemistry and catalyst design.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿16,680.00
6-(Piperidin-1-yl)pyridine-3-carbaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for creating compounds with potential anticancer, anti-inflammatory, and neuroprotective activities. Commonly employed in the preparation of nitrogen-containing heterocyclic systems through condensation or coupling reactions. Also utilized in agrochemical research for d

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for creating compounds with potential anticancer, anti-inflammatory, and neuroprotective activities. Commonly employed in the preparation of nitrogen-containing heterocyclic systems through condensation or coupling reactions. Also utilized in agrochemical research for designing new active ingredients. Its aldehyde group enables Schiff base formation, useful in coordination chemistry and catalyst design.

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