CAS 51229-51-7

1-[4-(Bromomethyl)phenyl]ethanone

Description:

1-[4-(Bromomethyl)phenyl]ethanone, with the CAS number 51229-51-7, is an organic compound characterized by its ketone functional group and a bromomethyl substituent on a phenyl ring. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and temperature. It has a molecular structure that includes a phenyl group attached to an ethanone moiety, which contributes to its reactivity and potential applications in organic synthesis. The presence of the bromomethyl group enhances its electrophilic character, making it useful in various chemical reactions, such as nucleophilic substitutions. Additionally, this compound may exhibit moderate to low solubility in water but is generally soluble in organic solvents like ethanol and dichloromethane. Its reactivity and functional groups make it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Safety precautions should be taken when handling this compound, as it may pose health risks due to the presence of bromine and its potential reactivity.

Formula: C₉H₉BrO

InChI: InChI=1/C9H9BrO/c1-7(11)9-4-2-8(6-10)3-5-9/h2-5H,6H2,1H3

SMILES: CC(=O)c1ccc(cc1)CBr

Synonyms:

• Ethanone, 1-[4-(bromomethyl)phenyl]-
• 1-(4-(Bromomethyl)Phenyl)Ethanone

1-(4-(Bromomethyl)phenyl)ethanone

CAS: 51229-51-7

Formula: C₉H₉BrO

Purity: 97%

Color and Shape: Solid

Molecular weight: 213.074

Ref: 10-F079582

1-(4-(Bromomethyl)phenyl)ethanone

CAS: 51229-51-7

Formula: C₉H₉BrO

Purity: 97%

Color and Shape: Solid

Molecular weight: 213.0712

Ref: IN-DA00DHVD

1-(4-(Bromomethyl)phenyl)ethanone

CAS: 51229-51-7

1-(4-(Bromomethyl)phenyl)ethanone

Purity: 99%

Molecular weight: 213.07116g/mol

Ref: 54-OR301151

1-(4-(Bromomethyl)phenyl)ethanone

CAS: 51229-51-7

1-(4-(Bromomethyl)phenyl)ethanone is a synthetic compound that has been used as an intermediate in the synthesis of other compounds. It can be used to synthesize stilbene derivatives, amines, and carbenes. One of its uses is the cross-coupling reaction with primary alcohols to form a triarylbismuth complex. This process is known as the Wittig reaction, which involves the formation of an aromatic ring via an intermediate carbene. The 1-(4-bromomethyl)phenyl ethanone can also be used to synthesize monomers, such as polymers and plastics.

Formula: C₉H₉BrO

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 213.07 g/mol

Ref: 3D-FB31399

1-(4-(Bromomethyl)phenyl)ethanone

Controlled Product

CAS: 51229-51-7

Applications 1-(4-(Bromomethyl)phenyl)ethanone is useful in the synthesis of series of dihydropyrimidine and thiopyrimidine derivatives as antiviral agents.
References Sari, O., et al.: Eur. J. Med. Chem., 104, 127-138 (2015)

Formula: C₉H₉BrO

Color and Shape: Neat

Molecular weight: 213.071

Ref: TR-B697458