CAS 728-84-7

2-Bromo-1,3-diphenyl-1,3-propanedione

Description:

2-Bromo-1,3-diphenyl-1,3-propanedione, with the CAS number 728-84-7, is an organic compound characterized by its structure, which features two phenyl groups and a bromine substituent on a propanedione backbone. This compound typically appears as a solid at room temperature and is known for its reactivity due to the presence of the bromine atom, which can participate in various chemical reactions, including nucleophilic substitutions. The diketone functional groups contribute to its ability to form enolates, making it useful in synthetic organic chemistry. It is often employed as an intermediate in the synthesis of more complex organic molecules. The compound's solubility is generally moderate in organic solvents, and it may exhibit distinct UV-Vis absorption characteristics due to the conjugated system formed by the phenyl groups. Safety precautions should be taken when handling this compound, as it may pose health risks if inhaled or ingested, and appropriate protective equipment should be used.

Formula: C₁₅H₁₁BrO₂

InChI: InChI=1S/C15H11BrO2/c16-13(14(17)11-7-3-1-4-8-11)15(18)12-9-5-2-6-10-12/h1-10,13H

InChI key: InChIKey=BYAJHZYXPBREEK-UHFFFAOYSA-N

SMILES: C(C(C(=O)C1=CC=CC=C1)Br)(=O)C2=CC=CC=C2

Synonyms:

• 1,3-Propanedione, 2-Bromo-1,3-Diphenyl-
• 2-Bromo-1,3-diphenyl-1,3-propanedione
• 2-Bromo-1,3-diphenyl-propane-1,3-dione
• 2-Bromo-1,3-diphenylpropan-1,3-dione
• Bromodibenzoylmethane
• Dibenzoylbromomethane
• NSC 32217
• NSC 404285
• α-Bromodibenzoylmethane

2-Bromo-1,3-diphenylpropane-1,3-dione

CAS: 728-84-7

Formula: C₁₅H₁₁BrO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 303.1506

Ref: IN-DA003GLZ

2-Bromo-1,3-diphenyl-1,3-propanedione

CAS: 728-84-7

2-Bromo-1,3-diphenyl-1,3-propanedione

Purity: 97%

Molecular weight: 303.15g/mol

Ref: 54-OR1006976

2-Bromo-1,3-diphenylpropane-1,3-dione

CAS: 728-84-7

2-Bromo-1,3-diphenylpropane-1,3-dione is a ligand that binds to metal ions. It has been used as an efficient method for the synthesis of phenyl groups in organic chemistry. 2-Bromo-1,3-diphenylpropane-1,3-dione was found to have a catalytic effect on reactions involving halides and phosphine. A study on the reaction mechanism revealed that 2-bromo-1,3-diphenylpropane-1,3-dione acts as an electron donor to phosphites and phosphines. The xray diffraction study showed that the ligand binds to metal ions through its phenyl groups.

Formula: C₁₅H₁₁BrO₂

Purity: Min. 95%

Molecular weight: 303.15 g/mol

Ref: 3D-FB53995

2-Bromo-1,3-diphenyl-propane-1,3-dione

CAS: 728-84-7

Formula: C₁₅H₁₁BrO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 303.155

Ref: 10-F345629