CAS 243455-57-4

5-(3-bromophenyl)-1,3-oxazole

Description:

5-(3-Bromophenyl)-1,3-oxazole is an organic compound characterized by its oxazole ring, which is a five-membered heterocyclic structure containing both nitrogen and oxygen atoms. The presence of a bromophenyl group at the 5-position of the oxazole ring contributes to its unique chemical properties, including potential reactivity and biological activity. This compound typically exhibits moderate solubility in organic solvents and may have limited solubility in water due to its hydrophobic aromatic character. The bromine substituent can influence the compound's electronic properties, making it a candidate for various chemical reactions, such as nucleophilic substitutions or coupling reactions. Additionally, compounds like this one are often studied for their potential applications in pharmaceuticals, agrochemicals, or materials science due to their ability to interact with biological systems or serve as intermediates in synthetic pathways. Safety and handling precautions should be observed, as halogenated compounds can pose environmental and health risks.

Formula: C₉H₆BrNO

InChI: InChI=1/C9H6BrNO/c10-8-3-1-2-7(4-8)9-5-11-6-12-9/h1-6H

SMILES: c1cc(cc(c1)Br)c1cnco1

Synonyms:

• Oxazole, 5-(3-bromophenyl)-
• 5-(3-Bromophenyl)-1,3-oxazole
• 5-(3-Bromo-phenyl)-oxazole
• 5-(3-Bromophenyl)-1,3-oxazole97%
• 5-(3-Brom-phenyl)-oxazole
• 5-(3-Bromophenyl)-1,3-oxazole 97%

5-(3-Bromophenyl)-1,3-oxazole

CAS: 243455-57-4

Formula: C₉H₆BrNO

Purity: 95%

Color and Shape: Solid

Molecular weight: 224.0540

Ref: IN-DA003M4G

5-(3-Bromophenyl)-1,3-oxazole

CAS: 243455-57-4

5-(3-Bromophenyl)-1,3-oxazole

Formula: C₉H₆BrNO

Purity: ≥95%

Color and Shape: Off-White Powder

Molecular weight: 224.05g/mol

Ref: 54-OR9727

5-(3-Bromophenyl)-1,3-oxazole

CAS: 243455-57-4

Formula: C₉H₆BrNO

Purity: 95%

Molecular weight: 224.057

Ref: 10-F067234

5-(3-Bromophenyl)-1,3-oxazole

CAS: 243455-57-4

5-(3-Bromophenyl)-1,3-oxazole is a carbamate that inhibits the activity of hydroxylase enzymes. 5-(3-Bromophenyl)-1,3-oxazole is used to study the role of hydroxylase enzymes in metabolism and as a chemical inhibitor for research purposes. It has been shown to inhibit human liver cytosols and cytosolic preparations from other species. The reaction mechanism for 5-(3-bromophenyl)-1,3-oxazole is unknown; it may bind to an active site on the hydroxylase enzyme or react with a nucleophile in the substrate's transition state. It has been shown that this carbamate can inhibit certain oxidases such as aldehyde oxidase, but not others such as alcohol oxidase or lactate oxidase.

Formula: C₉H₆BrNO

Purity: Min. 95%

Molecular weight: 224.05 g/mol

Ref: 3D-TJA45557