CAS 19434-34-5
:2-Phenoxybenzaldehyde
Description:
2-Phenoxybenzaldehyde, with the CAS number 19434-34-5, is an organic compound characterized by its aromatic structure, which consists of a phenoxy group (a phenyl ether) attached to a benzaldehyde moiety. This compound typically appears as a colorless to pale yellow liquid or solid, depending on the temperature and purity. It has a distinctive aromatic odor, characteristic of many aldehydes. 2-Phenoxybenzaldehyde is known for its role in organic synthesis, particularly in the production of various pharmaceuticals and agrochemicals. It exhibits moderate solubility in organic solvents such as ethanol and ether, while being less soluble in water due to its hydrophobic aromatic structure. The compound can undergo typical reactions associated with aldehydes, including oxidation and condensation reactions. Additionally, it may exhibit biological activity, making it of interest in medicinal chemistry. Safety precautions should be taken when handling this compound, as it may cause irritation to the skin and eyes.
Formula:C13H10O2
InChI:InChI=1S/C13H10O2/c14-10-11-6-4-5-9-13(11)15-12-7-2-1-3-8-12/h1-10H
InChI key:InChIKey=IMPIIVKYTNMBCD-UHFFFAOYSA-N
SMILES:O(C1=C(C=O)C=CC=C1)C2=CC=CC=C2
Synonyms:- 2-Phenoxybenzaldehyde 97%
- 2-Phenoxybenzenecarbaldehyde
- Benzaldehyde, 2-phenoxy-
- Benzaldehyde, o-phenoxy-
- O-Phenoxybenzaldehyde
- 2-Phenoxybenzaldehyde
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Found 5 products.
2-Phenoxybenzaldehyde
CAS:Formula:C13H10O2Purity:>96.0%(GC)Color and Shape:Colorless to Yellow clear liquidMolecular weight:198.222-Phenoxybenzaldehyde
CAS:2-PhenoxybenzaldehydeFormula:C13H10O2Purity:97%Color and Shape: slight yeloow. clear liquidMolecular weight:198.22g/mol2-Phenoxybenzaldehyde
CAS:<p>2-Phenoxybenzaldehyde is an organic compound that belongs to the heterocyclic aldehyde family. It is a white solid with a strong, pleasant odor. 2-Phenoxybenzaldehyde is used as an intermediate in organic synthesis, and has been shown to inhibit the receptor activity of human leukocyte antigen (HLA) class II molecules. The reaction mechanism for this inhibition is not known. The reaction of 2-phenoxybenzaldehyde with hydrochloric acid produces phenylhydroxylamine, which can be oxidized by inorganic acids to form phenyloxalic acid. This compound also inhibits the production of inflammatory cytokines such as TNFα and IL-1β in vitro and in vivo.</p>Formula:C13H10O2Purity:Min. 95%Color and Shape:Clear LiquidMolecular weight:198.22 g/mol




