CAS 6940-49-4
:3-Bromophthalide
Description:
3-Bromophthalide is an organic compound characterized by its structure, which features a phthalide core with a bromine substituent at the 3-position. It is a derivative of phthalide, a lactone that is known for its aromatic properties and is often used in organic synthesis. The presence of the bromine atom introduces both electrophilic and nucleophilic reactivity, making 3-bromophthalide a useful intermediate in various chemical reactions, including substitution and coupling reactions. This compound typically appears as a solid at room temperature and is soluble in organic solvents such as ethanol and dichloromethane. Its applications extend to the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, 3-bromophthalide may exhibit biological activity, which can be explored for potential therapeutic uses. As with many brominated compounds, it is important to handle 3-bromophthalide with care due to potential toxicity and environmental concerns associated with brominated organic compounds.
Formula:C8H5BrO2
InChI:InChI=1S/C8H5BrO2/c9-7-5-3-1-2-4-6(5)8(10)11-7/h1-4,7H
InChI key:InChIKey=CLMSHAWYULIVFQ-UHFFFAOYSA-N
SMILES:BrC1C=2C(C(=O)O1)=CC=CC2
Synonyms:- (±)-3-Bromo-1(3H)-isobenzofuranone
- 1(3H)-Isobenzofuranone, 3-bromo-
- 3-Bromo Phthalide
- 3-Bromo-1,3-dihydro-2-benzofuran-1-one
- 3-Bromo-3H-2-benzofuran-1-one
- 3-Bromo-3H-isobenzofuran-1-one
- 3-Bromophtalide
- 3-bromo-2-benzofuran-1(3H)-one
- NSC 60137
- Phthalide, 3-bromo-
- Phthalidyl bromide
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Found 8 products.
3-Bromophthalide
CAS:Formula:C8H5BrO2Purity:>98.0%(T)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:213.033-BroMoisobenzofuran-1(3H)-one
CAS:Formula:C8H5BrO2Purity:96%Color and Shape:SolidMolecular weight:213.02813-Bromophthalide
CAS:<p>3-Bromophthalide is a potent antibacterial agent that blocks the synthesis of fatty acids, leading to bacterial cell death. It can be used to treat metabolic disorders and heart disease. 3-Bromophthalide has an antibacterial action against many Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA) and Clostridium perfringens, but not against acid-fast bacteria such as Mycobacterium tuberculosis or Mycobacterium avium complex. The mechanism of antibacterial activity is due to its ability to inhibit the synthesis of fatty acids by blocking enzymes in the fatty acid biosynthetic pathway. 3-Bromophthalide also has antiinflammatory effects, which may be due to its ability to inhibit prostaglandin synthesis.</p>Formula:C8H5BrO2Purity:Min. 95%Molecular weight:213.03 g/mol
