CAS 7499-56-1

3-(2-Bromophenyl)-2-propenoic acid

Description:

3-(2-Bromophenyl)-2-propenoic acid, also known by its CAS number 7499-56-1, is an organic compound characterized by the presence of a propenoic acid moiety substituted with a bromophenyl group. This compound features a double bond between the second and third carbon atoms, which contributes to its reactivity, particularly in electrophilic addition reactions. The bromine atom on the aromatic ring enhances the compound's electrophilic character, making it useful in various synthetic applications. It is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. The presence of the carboxylic acid functional group imparts acidic properties, allowing it to participate in acid-base reactions. Additionally, the compound may exhibit biological activity, making it of interest in medicinal chemistry and material science. Its structural characteristics suggest potential applications in the synthesis of more complex organic molecules, as well as in the development of agrochemicals or pharmaceuticals. Safety data should be consulted for handling and storage, as halogenated compounds can pose health risks.

Formula: C₉H₇BrO₂

InChI: InChI=1S/C9H7BrO2/c10-8-4-2-1-3-7(8)5-6-9(11)12/h1-6H,(H,11,12)

InChI key: InChIKey=OMHDOOAFLCMRFX-UHFFFAOYSA-N

SMILES: C(=CC(O)=O)C1=C(Br)C=CC=C1

Synonyms:

• 2-Bromocinnamic acid
• 2-Propenoic acid, 3-(2-bromophenyl)-
• 3-(2-Bromophenyl)-2-propenoic acid
• 3-(2-Bromophenyl)acrylic acid
• Bromocinnamic Acid,2-
• Cinnamic acid, o-bromo-
• NSC 407679
• Rarechem Bk Hc T304
• o-Bromocinnamic acid

2-​Propenoic acid, 3-​(2-​bromophenyl)​-

CAS: 7499-56-1

Formula: C₉H₇BrO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 227.0547

Ref: IN-DA008OBS

2-Bromocinnamic Acid

CAS: 7499-56-1

2-Bromocinnamic Acid

Purity: 98%

Molecular weight: 227.05g/mol

Ref: 54-OR1030235

2-Bromocinnamic acid

CAS: 7499-56-1

2-Bromocinnamic acid is a synthetic compound that inhibits the reactions of arylating agents with tissues. It has cytotoxic activity and can be used in the treatment of alzheimer's disease. The synthesis of 2-bromocinnamic acid begins with anhydrous acetonitrile, which is heated to form an anhydrous salt. This salt is then dissolved in water and treated with potassium iodide and sodium nitrite. The resultant mixture undergoes a series of reactions to produce 2-bromocinnamic acid, including the addition of molybdenum as a catalyst. The reaction also produces byproducts that are removed by extraction or distillation. Finally, it undergoes a chromophore change from yellow to red in the presence of air due to oxidation by atmospheric oxygen.

Formula: C₉H₇BrO₂

Purity: Min. 95%

Molecular weight: 227.05 g/mol

Ref: 3D-FB19215

3-(2-Bromophenyl)acrylic acid

CAS: 7499-56-1

Purity: 97%

Molecular weight: 225.96

Ref: 10-F552204

2-Bromocinnamic Acid

Controlled Product

CAS: 7499-56-1

Applications 2-Bromocinnamic Acid (cas# 7499-56-1) is a compound useful in organic synthesis.
References Belley, M., et al.: Bioorg. Med. Chem. Lett., 15, 527 (2005),

Formula: C₉H₇BrO₂

Color and Shape: Neat

Molecular weight: 227.05

Ref: TR-B682430