2-Bromobenzaldehyde diethyl acetal

97%

Reagent Code: #116812
label
Alias 2-Bromobenzaldehyde diethyl acetal 1-bromo-2-(diethoxymethyl)benzene
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CAS Number 35822-58-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 259.14 g/mol
Formula C₁₁H₁₅BrO₂
badge Registry Numbers
EC Number 000-000-0
MDL Number MFCD01075696
thermostat Physical Properties
Boiling Point 116 °C0.7 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.285 g/mL at 25 °C(lit.)
Storage room temperature

description Product Description

This chemical is widely used in organic synthesis as a protective group for aldehydes. It is particularly valuable in multi-step reactions where the aldehyde functionality needs to be shielded from reactive conditions. The diethyl acetal group can be easily removed under acidic conditions, restoring the aldehyde for further transformations. It is also employed in the preparation of pharmaceuticals, agrochemicals, and fine chemicals, where it serves as an intermediate in the construction of complex molecules. Additionally, it finds use in the synthesis of heterocyclic compounds, which are important in medicinal chemistry and material science. Its stability and ease of deprotection make it a versatile reagent in synthetic organic chemistry.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (GC) 96.5-100%
Refractive Index (N20/D) 1.513-1.517
Specific Gravity (20/20) 1.286-1.29
Appearance Colorless Liquid
Infrared Spectrum Conforms to Structure
Proton NMR Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days $32.21
inventory 500g
10-20 days $1,374.08
inventory 25g
10-20 days $101.77
inventory 1g
10-20 days $14.17
inventory 100g
10-20 days $288.99
2-Bromobenzaldehyde diethyl acetal
This chemical is widely used in organic synthesis as a protective group for aldehydes. It is particularly valuable in multi-step reactions where the aldehyde functionality needs to be shielded from reactive conditions. The diethyl acetal group can be easily removed under acidic conditions, restoring the aldehyde for further transformations. It is also employed in the preparation of pharmaceuticals, agrochemicals, and fine chemicals, where it serves as an intermediate in the construction of complex molecules. Additionally, it finds use in the synthesis of heterocyclic compounds, which are important in medicinal chemistry and material science. Its stability and ease of deprotection make it a versatile reagent in synthetic organic chemistry.
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