3-Bromobenzaldehyde diethyl acetal
98%
Reagent
Code: #118094
Alias
3-Bromobenzaldehyde diethyl acetal
1-Bromo-3-(diethoxymethyl)benzene
3-Bromobenzaldehyde glyoxal
CAS Number
75148-49-1
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
MFCD01075697
thermostat
Physical Properties
Melting Point
95°C/1mm
Boiling Point
95 °C0.5 mm Hg(lit.)
inventory_2
Storage & Handling
Density
1.271 g/mL at 25 °C(lit.)
Storage
room temperature
description Product Description
Used primarily in organic synthesis as a protective group for aldehydes, it helps in preventing unwanted reactions during complex chemical processes. It is also employed in the production of pharmaceuticals and fine chemicals, where it acts as an intermediate in the synthesis of various active compounds. Additionally, it finds application in the development of agrochemicals, contributing to the creation of more effective and safer pesticides. Its role in research and development is significant, particularly in the study of organic reactions and the development of new synthetic methodologies.
format_list_bulleted Product Specification
| Test Parameter | Specification |
|---|---|
| Purity (GC) | 98-100% |
| Refractive Index (N20/D) | 1.51-1.514 |
| Specific Gravity (20/20) | 1.278-1.282 |
| Appearance | Liquid |
| Infrared Spectrum | Conforms to Structure |
| Proton NMR Spectrum | Conforms To Structure |
shopping_cart Available Sizes & Pricing
3-Bromobenzaldehyde diethyl acetal
Used primarily in organic synthesis as a protective group for aldehydes, it helps in preventing unwanted reactions during complex chemical processes. It is also employed in the production of pharmaceuticals and fine chemicals, where it acts as an intermediate in the synthesis of various active compounds. Additionally, it finds application in the development of agrochemicals, contributing to the creation of more effective and safer pesticides. Its role in research and development is significant, particularly in the study of organic reactions and the development of new synthetic methodologies.
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