CAS 25333-24-8

Methyl 3-Benzoylpropionate

Description:

Methyl 3-benzoylpropionate, with the CAS number 25333-24-8, is an organic compound characterized by its ester functional group. It features a propionate backbone with a benzoyl group attached to the third carbon, which contributes to its aromatic properties. This compound is typically a colorless to pale yellow liquid with a pleasant, sweet odor, making it useful in the fragrance and flavor industries. Methyl 3-benzoylpropionate is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic nature. It is known for its applications in organic synthesis, particularly as an intermediate in the production of various pharmaceuticals and agrochemicals. Additionally, it may exhibit UV-absorbing properties, which can be beneficial in cosmetic formulations. As with many organic compounds, safety precautions should be taken when handling it, as it may cause irritation to the skin and eyes. Proper storage in a cool, dry place away from light is recommended to maintain its stability and efficacy.

Formula: C₁₁H₁₂O₃

InChI: InChI=1/C11H12O3/c1-14-11(13)8-7-10(12)9-5-3-2-4-6-9/h2-6H,7-8H2,1H3

SMILES: COC(=O)CCC(=O)c1ccccc1

Synonyms:

• 3-Benzoylpropionic acid methyl ester
• Methyl 4-Oxo-4-Phenylbutanoate

Methyl 3-Benzoylpropionate

CAS: 25333-24-8

Formula: C₁₁H₁₂O₃

Purity: >98.0%(GC)

Color and Shape: White or Colorless to Light orange to Yellow powder to lump to clear liquid

Molecular weight: 192.21

Ref: 3B-B1546

Methyl 4-oxo-4-phenylbutanoate

CAS: 25333-24-8

Formula: C₁₁H₁₂O₃

Purity: 95%

Color and Shape: Liquid

Molecular weight: 192.2112

Ref: IN-DA003RRB

Methyl 3-benzoylpropionate

CAS: 25333-24-8

Methyl 3-benzoylpropionate

Purity: 98%

Molecular weight: 192.21g/mol

Ref: 54-OR918821

Methyl 3-Benzoylpropionate

CAS: 25333-24-8

Formula: C₁₁H₁₂O₃

Purity: 95%

Color and Shape: Liquid, Clear

Molecular weight: 192.214

Ref: 10-F341923

Methyl 3-Benzoylpropionate

CAS: 25333-24-8

Methyl 3-benzoylpropionate (MBAP) is an alkylating agent that is used in the synthesis of various drugs. MBAP reacts with an amine to form a pyridinium salt, which undergoes dehydrogenation, followed by alkylation. This reaction is catalyzed by the addition of chloride ions and olefinic compounds. The asymmetric synthesis of MBAP involves bromolactonization, followed by benzoylation. The structural analysis of MBAP was determined using NMR spectroscopy, which provides information about the stereochemistry of the molecule. The catalytic mechanism for MBAP was determined through X-ray crystallography and quantum chemical calculations.

Formula: C₁₁H₁₂O₃

Purity: Min. 95%

Molecular weight: 192.21 g/mol

Ref: 3D-ABA33324