Lithium acetoacetate

95%

Reagent Code: #202065
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Alias Lithium acetoacetate
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CAS Number 3483-11-2

science Other reagents with same CAS 3483-11-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 108.02 g/mol
Formula C₄H₅LiO₃
badge Registry Numbers
MDL Number MFCD00013060
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used as a reagent in organic synthesis, particularly in lithium enolate chemistry for carbon-carbon bond formation. It serves as a source of nucleophilic enolates in aldol-type reactions and Michael additions. Commonly employed in pharmaceutical intermediates synthesis where controlled enolization is required. Also utilized in coordination chemistry as a ligand precursor due to its ability to chelate metal ions. Its solubility in polar aprotic solvents makes it suitable for use in homogeneous reaction conditions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,270.00
inventory 1g
10-20 days ฿6,990.00
inventory 5g
10-20 days ฿25,390.00
inventory 25g
10-20 days ฿110,000.00

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Lithium acetoacetate
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Used as a reagent in organic synthesis, particularly in lithium enolate chemistry for carbon-carbon bond formation. It serves as a source of nucleophilic enolates in aldol-type reactions and Michael additions. Commonly employed in pharmaceutical intermediates synthesis where controlled enolization is required. Also utilized in coordination chemistry as a ligand precursor due to its ability to chelate metal ions. Its solubility in polar aprotic solvents makes it suitable for use in homogeneous reaction co

Used as a reagent in organic synthesis, particularly in lithium enolate chemistry for carbon-carbon bond formation. It serves as a source of nucleophilic enolates in aldol-type reactions and Michael additions. Commonly employed in pharmaceutical intermediates synthesis where controlled enolization is required. Also utilized in coordination chemistry as a ligand precursor due to its ability to chelate metal ions. Its solubility in polar aprotic solvents makes it suitable for use in homogeneous reaction conditions.

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