Triethyl methanetricarboxylate

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Reagent Code: #240588
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CAS Number 6279-86-3

science Other reagents with same CAS 6279-86-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.23 g/mol
Formula C₁₀H₁₆O₆
badge Registry Numbers
MDL Number MFCD00009150
thermostat Physical Properties
Melting Point 25-26°C (Lit.)
Boiling Point 253°C (Lit.)
inventory_2 Storage & Handling
Density 1.0950
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pyrazole and pyrrole derivatives, which are important structures in pharmaceuticals and agrochemicals. It participates in condensation reactions to form heterocyclic compounds due to the reactivity of its ester groups. Commonly employed in the synthesis of active pharmaceutical ingredients where a triester functionality acts as a building block for ring formation. Also utilized in the development of specialty chemicals requiring multifunctional ester precursors.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿360.00
inventory 25g
10-20 days ฿1,370.00
inventory 100g
10-20 days ฿5,370.00
inventory 500g
10-20 days ฿25,520.00

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Triethyl methanetricarboxylate
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Used as an intermediate in organic synthesis, particularly in the preparation of pyrazole and pyrrole derivatives, which are important structures in pharmaceuticals and agrochemicals. It participates in condensation reactions to form heterocyclic compounds due to the reactivity of its ester groups. Commonly employed in the synthesis of active pharmaceutical ingredients where a triester functionality acts as a building block for ring formation. Also utilized in the development of specialty chemicals requi

Used as an intermediate in organic synthesis, particularly in the preparation of pyrazole and pyrrole derivatives, which are important structures in pharmaceuticals and agrochemicals. It participates in condensation reactions to form heterocyclic compounds due to the reactivity of its ester groups. Commonly employed in the synthesis of active pharmaceutical ingredients where a triester functionality acts as a building block for ring formation. Also utilized in the development of specialty chemicals requiring multifunctional ester precursors.

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