Tetrahydrofuran-2-yl acetate

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Reagent Code: #57725
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CAS Number 1608-67-9

science Other reagents with same CAS 1608-67-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 130.14 g/mol
Formula C₆H₁₀O₃
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MDL Number MFCD09907739
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Tetrahydrofuran-2-yl acetate (2-acetoxytetrahydrofuran) is a specialty chemical and reactive intermediate primarily used in organic synthesis. It functions as a synthetic equivalent of succindialdehyde (in its cyclic acetal form), facilitating the Paal-Knorr synthesis of pyrroles, furans, and related heterocycles, as well as the preparation of porphyrins and other complex structures. It is also employed as a glycosyl donor in carbohydrate chemistry for synthesizing furanosides and in the production of pharmaceutical and agrochemical intermediates. Unlike common solvents, its value lies in its specific reactivity rather than broad solvency.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,872.00
inventory 250mg
10-20 days ฿16,290.00
inventory 1g
10-20 days ฿40,788.00

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Tetrahydrofuran-2-yl acetate
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Tetrahydrofuran-2-yl acetate (2-acetoxytetrahydrofuran) is a specialty chemical and reactive intermediate primarily used in organic synthesis. It functions as a synthetic equivalent of succindialdehyde (in its cyclic acetal form), facilitating the Paal-Knorr synthesis of pyrroles, furans, and related heterocycles, as well as the preparation of porphyrins and other complex structures. It is also employed as a glycosyl donor in carbohydrate chemistry for synthesizing furanosides and in the production of ph

Tetrahydrofuran-2-yl acetate (2-acetoxytetrahydrofuran) is a specialty chemical and reactive intermediate primarily used in organic synthesis. It functions as a synthetic equivalent of succindialdehyde (in its cyclic acetal form), facilitating the Paal-Knorr synthesis of pyrroles, furans, and related heterocycles, as well as the preparation of porphyrins and other complex structures. It is also employed as a glycosyl donor in carbohydrate chemistry for synthesizing furanosides and in the production of pharmaceutical and agrochemical intermediates. Unlike common solvents, its value lies in its specific reactivity rather than broad solvency.

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