CAS 642-29-5
:1-Benzoylnaphthalene
Description:
1-Benzoylnaphthalene, with the CAS number 642-29-5, is an organic compound that belongs to the class of ketones. It features a naphthalene ring substituted with a benzoyl group, which contributes to its unique chemical properties. This compound is typically a white to pale yellow crystalline solid with a characteristic aromatic odor. It is sparingly soluble in water but soluble in organic solvents such as ethanol and ether. 1-Benzoylnaphthalene is known for its applications in organic synthesis, particularly as a photoinitiator in polymerization processes and as a reagent in various chemical reactions. Its structure allows it to participate in electrophilic aromatic substitution reactions, making it a valuable intermediate in the synthesis of more complex organic molecules. Additionally, it exhibits fluorescence properties, which can be utilized in various analytical techniques. Safety precautions should be taken when handling this compound, as it may pose health risks if ingested or inhaled.
Formula:C17H12O
InChI:InChI=1S/C17H12O/c18-17(14-8-2-1-3-9-14)16-12-6-10-13-7-4-5-11-15(13)16/h1-12H
InChI key:InChIKey=CXAYOCVHDCXPAI-UHFFFAOYSA-N
SMILES:C(=O)(C=1C2=C(C=CC1)C=CC=C2)C3=CC=CC=C3
Synonyms:- (1-Naphthalenyl)phenyl methanone
- 1-Benzoylnaphthalene
- 1-Naphthalenylphenylmethanone
- 1-Naphthophenone
- Ai3-04214
- Benzoylnaphthalene
- Ketone, 1-naphthyl phenyl
- Methanone, 1-naphthalenylphenyl-
- NSC 6729
- Naphthalen-1-Yl(Phenyl)Methanone
- Naphthyl phenyl ketone
- Phenyl 1-naphthyl ketone
- α-Benzoylnaphthalene
- α-Naphthyl phenyl ketone
- See more synonyms
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Found 4 products.
Naphthalen-1-yl(phenyl)methanone
CAS:Formula:C17H12OPurity:98%Color and Shape:SolidMolecular weight:232.27661-Naphthyl phenyl ketone
CAS:1-Naphthyl phenyl ketoneFormula:C17H12OPurity:≥95%Color and Shape: off-white powderMolecular weight:232.28g/mol1-Naphthyl phenyl ketone
CAS:<p>1-Naphthyl phenyl ketone is a hydroxylated aromatic compound that has shown anticancer activity in leukemia cells. The 1-Naphthyl phenyl ketone molecule also possesses fluorescence properties, which are used for optical imaging. When 1-Naphthyl phenyl ketone is acylated with an electron-deficient alkylating agent such as methyl chloroformate, it forms the corresponding carbonyl compound, which can be used as a polymerization initiator in polymers. This reaction was first studied in detail by Otto Wallach and Heinrich Otto Wieland in 1891 and 1892. Radiation can also induce the decomposition of 1-naphthyl phenyl ketone to produce naphthalene.</p>Formula:C17H12OPurity:Min. 95%Molecular weight:232.28 g/mol



