CAS 4254-67-5
:1-[4-(benzyloxy)phenyl]-2-bromoethanone
Description:
1-[4-(Benzyloxy)phenyl]-2-bromoethanone, with the CAS number 4254-67-5, is an organic compound characterized by its unique structural features. It contains a bromine atom attached to an ethanone moiety, which is further substituted with a benzyloxy group and a phenyl ring. This compound typically exhibits a white to off-white crystalline appearance. It is soluble in organic solvents such as dichloromethane and ethanol but may have limited solubility in water due to its hydrophobic aromatic components. The presence of the bromine atom suggests potential reactivity, making it useful in various chemical synthesis applications, particularly in the formation of carbon-carbon bonds. Additionally, the benzyloxy group can serve as a protective group in organic synthesis. The compound's properties, such as melting point and boiling point, can vary based on purity and environmental conditions. Overall, 1-[4-(benzyloxy)phenyl]-2-bromoethanone is a valuable intermediate in organic chemistry, particularly in the synthesis of more complex molecules.
Formula:C15H13BrO2
InChI:InChI=1/C15H13BrO2/c16-10-15(17)13-6-8-14(9-7-13)18-11-12-4-2-1-3-5-12/h1-9H,10-11H2
SMILES:c1ccc(cc1)COc1ccc(cc1)C(=O)CBr
Synonyms:- Ethanone, 2-Bromo-1-[4-(Phenylmethoxy)Phenyl]-
- 1-[4-(Benzyloxy)phenyl]-2-bromoethanone
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Found 5 products.
4-(BENZYLOXY)-PHENACYL BROMIDE
CAS:Formula:C15H13BrO2Purity:95%Color and Shape:SolidMolecular weight:305.16651-(4-(Benzyloxy)phenyl)-2-bromoethanone
CAS:1-(4-(Benzyloxy)phenyl)-2-bromoethanonePurity:97%Molecular weight:305.17g/mol1-(4-(Benzyloxy)phenyl)-2-bromoethanone
CAS:Controlled ProductFormula:C15H13BrO2Color and Shape:NeatMolecular weight:305.1661-(4-(Benzyloxy)phenyl)-2-bromoethanone
CAS:<p>1-(4-Benzyloxy)phenyl-2-bromoethanone is a carbonylation agent that is used to synthesize alkaloids. This compound is efficient and can be used in the synthesis of rigidin, a tetrasubstituted benzene. It is also used as a reagent for the protection of benzyl groups. The deprotection reaction occurs by using triphosgene or catalytic hydrogenation.</p>Formula:C15H13BrO2Purity:Min. 95%Molecular weight:305.17 g/mol




