Cas no 3893-18-3 (4-Bromocinnamaldehyde)

4-Bromocinnamaldehyde is a brominated derivative of cinnamaldehyde, characterized by the presence of a bromine substituent at the para position of the aromatic ring. This compound is widely utilized as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals, agrochemicals, and fine chemicals. Its α,β-unsaturated aldehyde moiety makes it a versatile building block for Michael additions, condensation reactions, and other transformations. The bromine atom enhances reactivity, enabling selective functionalization. 4-Bromocinnamaldehyde is also employed in materials science for the synthesis of conjugated polymers and liquid crystals. Its high purity and stability ensure consistent performance in research and industrial applications.
4-Bromocinnamaldehyde structure
4-Bromocinnamaldehyde structure
Product Name:4-Bromocinnamaldehyde
CAS No:3893-18-3
MF:C9H7BrO
MW:211.055281877518
CID:924039
PubChem ID:6285035
Update Time:2025-06-07

4-Bromocinnamaldehyde Chemical and Physical Properties

Names and Identifiers

    • 4-Bromocinnamaldehyde
    • p-Br-cinnamaldehyde
    • trans-3-(4-Bromophenyl)acrylaldehyde
    • (2E)-3-(4-bromophenyl)prop-2-enal
    • (E)-3-(4-bromophenyl)prop-2-enal
    • A871752
    • B4337
    • 49678-04-8
    • trans-4-Bromocinnamaldehyde, 97%
    • (e)-3-(4-bromo-phenyl)-propenal
    • AS-40767
    • XYRAWLRFGKLUMW-OWOJBTEDSA-N
    • (E)-3-(4-Bromophenyl)acrylaldehyde
    • AM85792
    • J-011290
    • trans-4-Bromocinnamaldehyde
    • 3-(4-bromophenyl)acrylaldehyde
    • EN300-6493861
    • 3-(4-bromophenyl)-acrolein
    • J-501909
    • Z1269187977
    • trans-3-(4-Bromophenyl)acrolein
    • SCHEMBL240614
    • STK035164
    • (E)-3-(4-Bromophenyl)-2-propenal
    • trans-3-(4-Bromophenyl)-2-propenal
    • 2-Propenal, 3-(4-bromophenyl)-, (2E)-
    • 3893-18-3
    • SCHEMBL240615
    • CS-W015068
    • AKOS005128498
    • E-3-(4-Bromophenyl)-2-propenal
    • trans
    • -4-Bromocinnamaldehyde
    • Inchi: 1S/C9H7BrO/c10-9-5-3-8(4-6-9)2-1-7-11/h1-7H/b2-1+
    • InChI Key: XYRAWLRFGKLUMW-OWOJBTEDSA-N
    • SMILES: BrC1C=CC(/C=C/C=O)=CC=1

Computed Properties

  • Exact Mass: 209.96803g/mol
  • Monoisotopic Mass: 209.96803g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 2
  • Complexity: 146
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 1
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2.5
  • Topological Polar Surface Area: 17.1?2

Experimental Properties

  • Density: 1.5±0.1 g/cm3
  • Melting Point: 70-74°C
  • Boiling Point: 310.5±17.0 °C at 760 mmHg
  • Flash Point: 114.5±8.3 °C
  • Vapor Pressure: 0.0±0.7 mmHg at 25°C

4-Bromocinnamaldehyde Security Information

4-Bromocinnamaldehyde Pricemore >>

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4-Bromocinnamaldehyde Production Method

Production Method 1

Reaction Conditions
1.1R:F3CCO2H, R:NaNO2, S:CHCl3, 10-15 min, rt; 0-5°C; 5°C → 20°C; 1 h, 20°C
1.2C:Al2O3, 20°C
Reference
Isomerization of 3-unsubstituted 4,5-dihydroisoxazoles over alumina. A new synthesis of β-hydroxy nitriles
By Mochalov, S. S. et al, Russian Journal of Organic Chemistry, 2016, 52(3), 397-403

4-Bromocinnamaldehyde Raw materials

4-Bromocinnamaldehyde Preparation Products

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