Diethyl malonate

≥99.5%

Reagent Code: #176824
label
Alias Diethyl malonic acid; ethyl malonic acid, ethyl carrotate
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CAS Number 105-53-3

science Other reagents with same CAS 105-53-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 160.17 g/mol
Formula C₇H₁₂O₄
badge Registry Numbers
EC Number 203-305-9
MDL Number MFCD00009195
thermostat Physical Properties
Melting Point -50 °C
Boiling Point 199 °C(lit.)
inventory_2 Storage & Handling
Density 1.055 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used primarily in organic synthesis, especially in the preparation of barbiturates, which are central nervous system depressants with sedative and hypnotic effects. Serves as a key building block in the Knoevenagel condensation reaction to form α,β-unsaturated carbonyl compounds. Employed in the synthesis of various pharmaceuticals, dyes, and agrochemicals due to its active methylene group that readily undergoes alkylation. Also utilized in fragrance and flavor industries for creating ester-based aroma compounds. Acts as a precursor in the production of vitamins, such as vitamin B1 and B6. Its ability to form cyclic structures makes it valuable in the manufacture of polymers and specialty chemicals.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100g
10-20 days ฿620.00
inventory 500g
10-20 days ฿1,760.00
inventory 2.5kg
10-20 days ฿6,660.00
inventory 10kg
10-20 days ฿13,490.00

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Diethyl malonate
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Used primarily in organic synthesis, especially in the preparation of barbiturates, which are central nervous system depressants with sedative and hypnotic effects. Serves as a key building block in the Knoevenagel condensation reaction to form α,β-unsaturated carbonyl compounds. Employed in the synthesis of various pharmaceuticals, dyes, and agrochemicals due to its active methylene group that readily undergoes alkylation. Also utilized in fragrance and flavor industries for creating ester-based aroma c

Used primarily in organic synthesis, especially in the preparation of barbiturates, which are central nervous system depressants with sedative and hypnotic effects. Serves as a key building block in the Knoevenagel condensation reaction to form α,β-unsaturated carbonyl compounds. Employed in the synthesis of various pharmaceuticals, dyes, and agrochemicals due to its active methylene group that readily undergoes alkylation. Also utilized in fragrance and flavor industries for creating ester-based aroma compounds. Acts as a precursor in the production of vitamins, such as vitamin B1 and B6. Its ability to form cyclic structures makes it valuable in the manufacture of polymers and specialty chemicals.

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