2-Bromobenzaldehyde diethyl acetal
97%
Reagent
Code: #116812
Alias
2-Bromobenzaldehyde diethyl acetal 1-bromo-2-(diethoxymethyl)benzene
CAS Number
35822-58-3
blur_circular Chemical Specifications
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Molecular Information
Weight
259.14 g/mol
Formula
C₁₁H₁₅BrO₂
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Registry Numbers
EC Number
000-000-0
MDL Number
MFCD01075696
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Physical Properties
Boiling Point
116 °C0.7 mm Hg(lit.)
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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 |
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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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