Cas no 15795-20-7 (Ethyl 3-(4-Bromophenyl)acrylate)

Ethyl 3-(4-Bromophenyl)acrylate is a brominated aromatic acrylate ester commonly utilized as a versatile intermediate in organic synthesis and pharmaceutical research. Its key advantages include a reactive α,β-unsaturated carbonyl group, enabling participation in Michael additions, cyclizations, and cross-coupling reactions. The 4-bromophenyl moiety enhances its utility in palladium-catalyzed transformations, such as Suzuki-Miyaura couplings, facilitating the construction of complex biaryl structures. The ethyl ester group offers improved solubility in organic solvents compared to free acids, simplifying handling and purification. This compound is particularly valuable in the development of fine chemicals, agrochemicals, and bioactive molecules, where its structural features enable precise functionalization. High purity grades ensure consistent performance in demanding synthetic applications.
Ethyl 3-(4-Bromophenyl)acrylate structure
15795-20-7 structure
Product Name:Ethyl 3-(4-Bromophenyl)acrylate
CAS No:15795-20-7
MF:C11H11BrO2
MW:255.107842683792
MDL:MFCD00012226
CID:1056416
PubChem ID:688115
Update Time:2025-05-20

Ethyl 3-(4-Bromophenyl)acrylate Chemical and Physical Properties

Names and Identifiers

    • Ethyl 3-(4-Bromophenyl)acrylate
    • (E)-3-(4-bromo-phenyl)-acrylic acid ethyl ester
    • ethyl p-bromocinnamate
    • Ethyl 3-(4-bromophenyl)-2-propenoate
    • CS-0047571
    • DS-5470
    • SCHEMBL69276
    • 2-Propenoic acid, 3-(4-bromophenyl)-, ethyl ester, (2E)-
    • (E)-ethyl 3-(4-bromo-phenyl)-acrylate
    • Ethyl3-(4-bromophenyl)acrylate
    • ethyl (E)-3-(4-bromophenyl)prop-2-enoate
    • NSC-636702
    • AB7158
    • Ethyl trans-4-bromocinnamate
    • NSC 636702
    • 24393-53-1
    • NSC636702
    • 15795-20-7
    • CHEMBL4877242
    • E-3-(4-bromo-phenyl)-acrylic acid ethyl ester
    • ETHYL 4-BROMOCINNAMATE
    • ethyl (E)-4-bromocinnamate
    • Ethyl-3-(4-bromophenyl)acrylate
    • A877940
    • ethyl (E)-3-(4-bromophenyl)acrylate
    • ZAA39353
    • Cinnamic acid, p-bromo-, ethyl ester
    • ethyl (2E)-3-(4-bromophenyl)prop-2-enoate
    • MFCD00012226
    • 2-Propenoic acid, 3-(4-bromophenyl)-, ethyl ester
    • Ethyl trans-4-bromocinnamate, 98%
    • J-015491
    • A921882
    • (E)-Ethyl 3-(4-bromophenyl)acrylate
    • AS-75660
    • ethyl-trans-4-bromocinnamate
    • (E)-Ethyl 3-(4-bromophenyl)acrylate, stabilized with MEHQ
    • EN300-1453798
    • AKOS015894025
    • ethyl (2E)-3-(4-bromophenyl)acrylate
    • MDL： MFCD00012226
    • Inchi： 1S/C11H11BrO2/c1-2-14-11(13)8-5-9-3-6-10(12)7-4-9/h3-8H,2H2,1H3/b8-5+
    • InChI Key： YOOKYIPLSLPRTC-VMPITWQZSA-N
    • SMILES： BrC1C=CC(/C=C/C(=O)OCC)=CC=1

Computed Properties

  • Exact Mass: 253.99423
  • Monoisotopic Mass: 253.99424g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 4
  • Complexity: 205
  • 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: 3.7
  • Topological Polar Surface Area: 26.3?2

Experimental Properties

  • PSA: 26.3

Ethyl 3-(4-Bromophenyl)acrylate Pricemore >>

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