CAS 66033-76-9

1,2-Benzisoxazole, 5-bromo-3-methyl-

Description:

1,2-Benzisoxazole, 5-bromo-3-methyl- is a heterocyclic organic compound characterized by its fused benzene and isoxazole rings. The presence of a bromine atom at the 5-position and a methyl group at the 3-position contributes to its unique chemical properties. This compound typically exhibits moderate solubility in organic solvents and may have limited solubility in water due to its hydrophobic aromatic structure. It is often utilized in medicinal chemistry and material science due to its potential biological activity and ability to participate in various chemical reactions, such as electrophilic substitutions and nucleophilic additions. The bromine substituent can enhance the compound's reactivity and influence its interaction with biological targets. Additionally, 1,2-benzisoxazoles are known for their applications in the development of pharmaceuticals, agrochemicals, and dyes, making them significant in both industrial and research settings. Safety and handling precautions should be observed, as with many halogenated compounds, due to potential toxicity and environmental impact.

Formula: C₈H₆BrNO

5-Bromo-3-methyl-1,2-benzoxazole

CAS: 66033-76-9

Formula: C₈H₆BrNO

Purity: 96%

Color and Shape: Solid

Molecular weight: 212.0433

Ref: IN-DA00FBXB

5-Bromo-3-methylbenzo[d]isoxazole

CAS: 66033-76-9

5-Bromo-3-methylbenzo[d]isoxazole

Purity: 98%

Molecular weight: 212.04g/mol

Ref: 54-OR94293

5-Bromo-3-methylbenzo[d]isoxazole

CAS: 66033-76-9

Formula: C₈H₆BrNO

Purity: 96%

Color and Shape: Solid, No data available.

Molecular weight: 212.046

Ref: 10-F454881

5-Bromo-3-methyl-1,2-benzoxazole

CAS: 66033-76-9

5-Bromo-3-methyl-1,2-benzoxazole is a chemical compound that can be synthesized by reacting 5-bromoindazole with methyl iodide. This chemical has been shown to react with hypochlorite in the presence of base to produce reactive oxygen species. Reactive oxygen species are known to cause cell death and DNA damage. 5-Bromo-3-methyl-1,2-benzoxazole has also been shown to undergo cyclisation upon reaction with sodium hypochlorite.

Formula: C₈H₆BrNO

Purity: Min. 95%

Molecular weight: 212.04 g/mol

Ref: 3D-RCA03376