3-Bromobenzaldehyde diethyl acetal

98%

  • Product Code: 118094
  Alias:    3-Bromobenzaldehyde diethyl acetal 1-Bromo-3-(diethoxymethyl)benzene 3-Bromobenzaldehyde glyoxal
  CAS:    75148-49-1
Molecular Weight: 259.14 g./mol Molecular Formula: C₁₁H₁₅BrO₂
EC Number: 000-000-0 MDL Number: MFCD01075697
Melting Point: 95°C/1mm Boiling Point: 95 °C0.5 mm Hg(lit.)
Density: 1.271 g/mL at 25 °C(lit.) Storage Condition: room temperature
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.
Product Specification:
Test 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
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days $12.04
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5.000 10-20 days $19.93
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25.000 10-20 days $71.43
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100.000 10-20 days $248.34
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500.000 10-20 days $1,024.94
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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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