Diacetonefructose

99%

Reagent Code: #169907
label
Alias 2,3:4,5-di-O-isopropylene-β-D-fructose; fructose diacetone
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CAS Number 20880-92-6

science Other reagents with same CAS 20880-92-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 260.28 g/mol
Formula C₁₂H₂₀O₆
badge Registry Numbers
MDL Number MFCD00022183
thermostat Physical Properties
Melting Point 94-95°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in organic synthesis, particularly in the production of specialty chemicals and pharmaceuticals. It serves as a building block for synthesizing heterocyclic compounds and can be employed in the development of chiral catalysts due to its structural features. Its keto-enol tautomerism makes it useful in studies involving reaction mechanisms and stereochemistry. Additionally, it finds application in the formulation of certain resins and functional polymers where controlled reactivity and solubility are required.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿300.00
5g
10-20 days ฿340.00
25g
10-20 days ฿1,160.00
100g
10-20 days ฿3,250.00
2.5kg
10-20 days ฿42,890.00
500g
10-20 days ฿11,900.00
Diacetonefructose
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Used primarily as an intermediate in organic synthesis, particularly in the production of specialty chemicals and pharmaceuticals. It serves as a building block for synthesizing heterocyclic compounds and can be employed in the development of chiral catalysts due to its structural features. Its keto-enol tautomerism makes it useful in studies involving reaction mechanisms and stereochemistry. Additionally, it finds application in the formulation of certain resins and functional polymers where controlled

Used primarily as an intermediate in organic synthesis, particularly in the production of specialty chemicals and pharmaceuticals. It serves as a building block for synthesizing heterocyclic compounds and can be employed in the development of chiral catalysts due to its structural features. Its keto-enol tautomerism makes it useful in studies involving reaction mechanisms and stereochemistry. Additionally, it finds application in the formulation of certain resins and functional polymers where controlled reactivity and solubility are required.

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