CAS 2567-29-5

Bromoethylbiphenyl

Description:

Bromoethylbiphenyl, with the CAS number 2567-29-5, is an organic compound characterized by the presence of a biphenyl structure substituted with a bromoethyl group. This compound typically exhibits a non-polar nature due to its aromatic biphenyl backbone, which contributes to its hydrophobic properties. The bromoethyl substituent introduces both bromine and ethyl functionalities, which can influence its reactivity and solubility in various solvents. Bromoethylbiphenyl may participate in electrophilic aromatic substitution reactions due to the electron-withdrawing nature of the bromine atom, making it a potential candidate for further chemical transformations. Its physical properties, such as melting point, boiling point, and density, are influenced by the molecular structure and substituents. Additionally, this compound may have applications in organic synthesis, materials science, or as an intermediate in the production of other chemical entities. Safety data should be consulted for handling and storage, as halogenated compounds can pose environmental and health risks.

Formula: C₁₃H₁₁Br

InChI: InChI=1/C13H11Br/c14-10-11-6-8-13(9-7-11)12-4-2-1-3-5-12/h1-9H,10H2

SMILES: c1ccc(cc1)c1ccc(cc1)CBr

Synonyms:

• 4-Bromoethylbiphenyl
• 4-(Bromomethyl)biphenyl
• 4-Phenylbenzyl bromide

4-BROMOMETHYLBIPHENYL

CAS: 2567-29-5

Formula: C₁₃H₁₁Br

Purity: 98%

Color and Shape: Solid

Molecular weight: 247.1304

Ref: IN-DA003L09

4-Bromomethylbiphenyl

CAS: 2567-29-5

Formula: C₁₃H₁₁Br

Purity: >98.0%(GC)

Color and Shape: White to Almost white powder to crystal

Molecular weight: 247.14

Ref: 3B-B1847

4-Bromomethyl-biphenyl

CAS: 2567-29-5

4-Bromomethyl-biphenyl

Formula: C₁₃H₁₁Br

Purity: 97%

Color and Shape: pale yellow solid

Molecular weight: 247.13g/mol

Ref: 54-OR315762

4-(Bromomethyl)biphenyl

CAS: 2567-29-5

4-(Bromomethyl)biphenyl is a biphenyl with a linear response to light. It has been shown to have high activity in hydrocarbon solvents, and can be used as a transfer agent. The reaction mechanism of 4-(Bromomethyl)biphenyl involves an alkoxycarbonyl group that reacts with an electron-deficient aromatic ring and the bromide ion (Br-) to produce the final product. The nmr spectra of this compound show the presence of hydrophilic compounds. 4-(Bromomethyl)biphenyl can be detected by liquid chromatography.

Formula: C₁₃H₁₁Br

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 247.13 g/mol

Ref: 3D-FB19258

4-Biphenylmethylbromide

CAS: 2567-29-5

Formula: C₁₃H₁₁Br

Purity: 95.0%

Color and Shape: Solid, Crystalline Powder

Molecular weight: 247.135

Ref: 10-F211928

4-(Bromomethyl)biphenyl

Controlled Product

CAS: 2567-29-5

Applications 4-(Bromomethyl)biphenyl is a biphenyl derivative used in the preparation of various pharmaceutical compounds such as protein tyrosine phosphatase 1B inhibitors. 4-(Bromomethyl)biphenyl is useful as as atom transfer radical polymerization initiator.
References Xie, J. et al.: Bioorg. Med. Chem. Lett., 21, 4306 (2011);

Formula: C₁₃H₁₁Br

Color and Shape: Neat

Molecular weight: 247.13

Ref: TR-B685295