CAS 877-35-0

2-bromo-1-phenylbutan-1-one

Description:

2-Bromo-1-phenylbutan-1-one, with the CAS number 877-35-0, is an organic compound characterized by its structure, which includes a bromine atom, a phenyl group, and a ketone functional group. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and temperature. It is known for its reactivity due to the presence of the bromine atom, which can participate in nucleophilic substitution reactions. The ketone functional group contributes to its potential as a precursor in organic synthesis, particularly in the formation of various derivatives through reactions such as reduction or condensation. Additionally, the phenyl group enhances its aromatic properties, which can influence its solubility and interaction with other chemical species. Safety considerations should be taken into account when handling this compound, as it may pose health risks if inhaled or ingested. Proper storage and handling protocols are essential to ensure safety in laboratory settings.

Formula: C₁₀H₁₁BrO

InChI: InChI=1/C10H11BrO/c1-2-9(11)10(12)8-6-4-3-5-7-8/h3-7,9H,2H2,1H3

SMILES: CCC(C(=O)c1ccccc1)Br

Synonyms:

• Alpha-Bromobutyrophenone

2-Bromo-1-phenylbutan-1-one

CAS: 877-35-0

Formula: C₁₀H₁₁BrO

Purity: 97%

Color and Shape: Liquid

Molecular weight: 227.0977

Ref: IN-DA00GWJA

a-Bromobutyrophenone

CAS: 877-35-0

Applications α-Bromobutyrophenone (cas# 877-35-0) is a compound useful in organic synthesis.

Formula: C₁₀H₁₁BrO

Color and Shape: Neat

Molecular weight: 227.0977

Ref: TR-B545090

2-Bromo-1-phenylbutan-1-one

CAS: 877-35-0

2-Bromo-1-phenylbutan-1-one is a copper salt that yields an acceptor in the presence of acetonitrile. It is used as a diagnostic agent, yielding a blue color when reacted with diazonium salt. 2-Bromo-1-phenylbutan-1-one also reacts with dopamine to form the diagnostic dye 2,6 dibromopurpurin. This compound has been shown to be cytotoxic for mammary cancer cells and other cancer cells, but not for healthy cells. The mechanism of action of this compound may involve sulfate and copper ions, which are required for its activity.

Formula: C₁₀H₁₁BrO

Purity: Min. 95%

Molecular weight: 227.1 g/mol

Ref: 3D-AAA87735