1,1,3,3-Tetramethoxypropane

98%

Reagent Code: #113955
label
Alias 1,1,3,3-Tetramethoxypropane; Malondialdehyde dimethyl acetal
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CAS Number 102-52-3

science Other reagents with same CAS 102-52-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 164.2 g/mol
Formula C₇H₁₆O₄
badge Registry Numbers
EC Number 203-037-2
MDL Number MFCD00008488
thermostat Physical Properties
Boiling Point 183 °C(lit.)
inventory_2 Storage & Handling
Density 0.997 g/mL at 25 °C(lit.)
Storage room temperature, dry

description Product Description

1,1,3,3-Tetramethoxypropane, also known as malonaldehyde bis(dimethyl acetal), is primarily used as a protected form of malonaldehyde in organic synthesis. It serves as a key intermediate for introducing the 1,3-dicarbonyl functionality in the preparation of heterocyclic compounds, such as pyrimidines and pyridines, which are essential in pharmaceuticals and agrochemicals. It facilitates reactions like carbon-carbon bond formation and ring closures in research laboratories. Additionally, it is employed in the development of complex organic molecules and drug intermediates.

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Test Parameter Specification
Purity (GC) 98-100
Refractive Index (N20/D) 1.406-1.409
Specific Gravity (20/20) 0.993-0.997
Appearance Colorless Liquid
Infrared Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 2.5L
10-20 days ฿7,190.00
inventory 25ml
10-20 days ฿350.00
inventory 100ml
10-20 days ฿680.00
inventory 500ml
10-20 days ฿1,890.00
inventory 100ml
10-20 days ฿750.00

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1,1,3,3-Tetramethoxypropane
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1,1,3,3-Tetramethoxypropane, also known as malonaldehyde bis(dimethyl acetal), is primarily used as a protected form of malonaldehyde in organic synthesis. It serves as a key intermediate for introducing the 1,3-dicarbonyl functionality in the preparation of heterocyclic compounds, such as pyrimidines and pyridines, which are essential in pharmaceuticals and agrochemicals. It facilitates reactions like carbon-carbon bond formation and ring closures in research laboratories. Additionally, it is employed in t
1,1,3,3-Tetramethoxypropane, also known as malonaldehyde bis(dimethyl acetal), is primarily used as a protected form of malonaldehyde in organic synthesis. It serves as a key intermediate for introducing the 1,3-dicarbonyl functionality in the preparation of heterocyclic compounds, such as pyrimidines and pyridines, which are essential in pharmaceuticals and agrochemicals. It facilitates reactions like carbon-carbon bond formation and ring closures in research laboratories. Additionally, it is employed in the development of complex organic molecules and drug intermediates.
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