Di-tert-butyl 2,6-dimethylpyridine-3,5-dicarboxylate

98%

Reagent Code: #130167
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CAS Number 55536-75-9

science Other reagents with same CAS 55536-75-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 307.38 g/mol
Formula C₁₇H₂₅NO₄
thermostat Physical Properties
Melting Point 108-109 °C(Solv: ethanol (64-17-5); water (7732-18-5))
Boiling Point 354.6±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.059±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators. It serves as a building block in medicinal chemistry due to the steric protection offered by the tert-butyl groups, which enhances stability during multi-step reactions. Commonly employed in the preparation of bioactive molecules and heterocyclic compounds where controlled functionalization of the pyridine core is required. Also utilized in research settings for designing catalysts and ligands in asymmetric synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,910.00
inventory 250mg
10-20 days ฿6,630.00
inventory 1g
10-20 days ฿17,890.00

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Di-tert-butyl 2,6-dimethylpyridine-3,5-dicarboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators. It serves as a building block in medicinal chemistry due to the steric protection offered by the tert-butyl groups, which enhances stability during multi-step reactions. Commonly employed in the preparation of bioactive molecules and heterocyclic compounds where controlled functionalization of the pyridine core is required. Also utilized in research settings for designing cata

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators. It serves as a building block in medicinal chemistry due to the steric protection offered by the tert-butyl groups, which enhances stability during multi-step reactions. Commonly employed in the preparation of bioactive molecules and heterocyclic compounds where controlled functionalization of the pyridine core is required. Also utilized in research settings for designing catalysts and ligands in asymmetric synthesis.

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