6'-Methoxy-2'-acetonaphthone

CAS : 3900-45-6

Ref. 3D-IM25222

Informations sur le produit

• Nom: 6'-Methoxy-2'-acetonaphthone
• Synonymes: 1-(6-Methoxy-2-naphthalenyl)ethanoneNaproxen impurity L, 1-(2-Methoxynaphthalen-6-yl)ethanone, 1-(6-Methoxy-2-naphthalenyl)-1-ethanone, 1-(6-Methoxy-2-naphthalenyl)ethanone, 1-(6-Methoxy-2-naphthyl)-1-ethanone, 1-(6-Methoxy-2-naphthyl)ethan-1-one, 1-(6-Methoxy-2-naphthyl)ethanone, 2-Methoxy-6-acetylnaphthalene, 2′-Acetonaphthone, 6′-methoxy-, 6-Acetyl-2-methoxynaphthalene, 6-Methoxy-2-acetonaphthone, 6-Methoxy-2-acetylnaphthalene, 6-Methoxy-2-naphthyl methyl ketone, Ethanone, 1-(6-methoxy-2-naphthalenyl)-, NSC 105564
• CAS: 3900-45-6

Description

6'-Methoxy-2'-acetonaphthone is a reactive chemical that can be used as a reagent in organic synthesis. It is an electron-rich aromatic compound and its reactivity is enhanced by electron-donating groups such as -OH, -NH2, or -SH. 6'-Methoxy-2'-acetonaphthone can be used to form new carbon-carbon bonds in the presence of metal catalysts. This reaction can be done in either the presence or absence of a solvent, although the yield is better when carried out in organic solvents. Oxime derivatives are formed as oxidation products during this reaction. Acetylation may also occur, which would produce acetophenones or phenylacetones.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 200.23 g/mol
• Formule: C₁₃H₁₂O₂
• Degré de pureté: Min. 95%
• Couleur/Forme: Off-White Powder
• InChI: InChI=1S/C13H12O2/c1-9(14)10-3-4-12-8-13(15-2)6-5-11(12)7-10/h3-8H,1-2H3
• Code InChI: InChIKey=GGWCZBGAIGGTDA-UHFFFAOYSA-N
• SMILES: COc1ccc2cc(C(C)=O)ccc2c1