O-Formyl Acetate

98%

Reagent Code: #221984
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CAS Number 2258-42-6

science Other reagents with same CAS 2258-42-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 88.06 g/mol
Formula C₃H₄O₃
badge Registry Numbers
MDL Number MFCD13184316
inventory_2 Storage & Handling
Storage -20°C, Inert Gas, Sealed, Drying

description Product Description

O-Formyl acetate is primarily used as an intermediate in organic synthesis, particularly in the preparation of esters and carboxylic acid derivatives. It serves as a reagent for introducing acyl groups in pharmaceutical and agrochemical manufacturing. Due to its reactivity, it is employed in acetylation and formylation reactions, enabling the modification of alcohols, amines, and other nucleophiles. Its role as a dual-functionalizing agent allows for sequential transformations in multi-step syntheses, making it valuable in the development of complex molecules. Additionally, it finds use in research laboratories for studying reaction mechanisms involving mixed anhydrides.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿5,360.00
inventory 1g
10-20 days ฿9,620.00
inventory 5g
10-20 days ฿31,760.00
O-Formyl Acetate
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O-Formyl acetate is primarily used as an intermediate in organic synthesis, particularly in the preparation of esters and carboxylic acid derivatives. It serves as a reagent for introducing acyl groups in pharmaceutical and agrochemical manufacturing. Due to its reactivity, it is employed in acetylation and formylation reactions, enabling the modification of alcohols, amines, and other nucleophiles. Its role as a dual-functionalizing agent allows for sequential transformations in multi-step syntheses, ma

O-Formyl acetate is primarily used as an intermediate in organic synthesis, particularly in the preparation of esters and carboxylic acid derivatives. It serves as a reagent for introducing acyl groups in pharmaceutical and agrochemical manufacturing. Due to its reactivity, it is employed in acetylation and formylation reactions, enabling the modification of alcohols, amines, and other nucleophiles. Its role as a dual-functionalizing agent allows for sequential transformations in multi-step syntheses, making it valuable in the development of complex molecules. Additionally, it finds use in research laboratories for studying reaction mechanisms involving mixed anhydrides.

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