CAS 19652-33-6
:5-Bromo-3-chloro-2-hydroxybenzaldehyde
Description:
5-Bromo-3-chloro-2-hydroxybenzaldehyde, with the CAS number 19652-33-6, is an organic compound characterized by its aromatic structure, which includes a benzaldehyde functional group. This compound features a hydroxyl group (-OH), a bromine atom, and a chlorine atom attached to the benzene ring, contributing to its unique reactivity and properties. The presence of these halogen substituents can influence the compound's polarity, solubility, and potential for hydrogen bonding. Typically, such compounds exhibit moderate to high reactivity due to the electrophilic nature of the aldehyde group and the electron-withdrawing effects of the halogens. This substance may be utilized in various chemical syntheses, particularly in the development of pharmaceuticals or agrochemicals, owing to its functional groups that can participate in further chemical reactions. Additionally, its physical properties, such as melting point and boiling point, would be influenced by the substituents and the overall molecular structure, making it an interesting compound for study in organic chemistry.
Formula:C7H4BrClO2
InChI:InChI=1S/C7H4BrClO2/c8-5-1-4(3-10)7(11)6(9)2-5/h1-3,11H
InChI key:InChIKey=XXFFEGBFFXHMTF-UHFFFAOYSA-N
SMILES:C(=O)C1=C(O)C(Cl)=CC(Br)=C1
Synonyms:- Salicylaldehyde, 5-bromo-3-chloro-
- 5-Bromo-3-chlorosalicylaldehyde
- 5-Bromo-3-chloro-2-hydroxybenzaldehyde
- Benzaldehyde, 5-bromo-3-chloro-2-hydroxy-
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Found 4 products.
5-Bromo-3-chloro-2-hydroxybenzaldehyde
CAS:Formula:C7H4BrClO2Purity:98%Color and Shape:SolidMolecular weight:235.46255-Bromo-3-chloro-2-hydroxybenzaldehyde
CAS:5-Bromo-3-chloro-2-hydroxybenzaldehydeFormula:C7H4BrClO2Purity:≥95%Color and Shape:SolidMolecular weight:235.46g/mol5-Bromo-3-chloro-2-hydroxybenzaldehyde
CAS:Formula:C7H4BrClO2Purity:98%Color and Shape:No data available.Molecular weight:235.465-Bromo-3-chloro-2-hydroxybenzaldehyde
CAS:<p>5-Bromo-3-chloro-2-hydroxybenzaldehyde is a potent regulator of microglia, a type of immune cell. It has been shown to be neuroprotective in the presence of radiation and activated TNF-α, by decreasing necrosis and inflammation. This compound is also capable of inhibiting the production of IL-1β and IL-6 from human monocytes, which may be due to its hydrophobic properties. 5-Bromo-3-chloro-2-hydroxybenzaldehyde has been shown to suppress the development of experimental sclerosis in rats. The mechanism for this effect is unknown, but it may be due to its ability to inhibit the activation of proinflammatory genes such as p65 nuclear translocation or nuclear factor kappa B (NFκB).</p>Formula:C7H4BrClO2Purity:Min. 95%Molecular weight:235.46 g/mol



