15540-09-7

Basic information

• Product Name: 3-Hexanone, 1-(4-methoxyphenyl)-5-methyl-
• CAS NO: 15540-09-7
• Molecular Formula: C14H20O2
• Molecular Weight: 220.312
• Mol File: 15540-09-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-Hexanone, 1-(4-methoxyphenyl)-5-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Hexanone, 1-(4-methoxyphenyl)-5-methyl-(15540-09-7)
• EPA Substance Registry System: 3-Hexanone, 1-(4-methoxyphenyl)-5-methyl-(15540-09-7)

Safety Data

• Hazardous Substances Data: 15540-09-7(Hazardous Substances Data)

Upstream product

• 82297-68-5 (E)-1-(4-methoxyphenyl)-5-methylhex-1-en-3-one 
• 1929-29-9 3-(4-methoxyphenyl)propanoic acid 
• 714957-46-7 1-hydroxy-1-(4-methoxy-phenyl)-5-methyl-hexan-3-one 
• 108-10-1 4-methyl-2-pentanone 
• 123-11-5 4-methoxy-benzaldehyde 
• 44396-74-9 isobutylzinc iodide 
• 208453-06-9 3-(4-methoxyphenyl)propionic acid ethanethiol ester 
• 72178-64-4 p-Methoxy-styryl-isobutyl-keton 

Downstream Products

• 26496-86-6 1-(4-methoxy phenyl) 5-methyl hexan-3-ol 
• 714957-47-8 1-(3-bromo-5-methyl-hexyl)-4-methoxy-benzene 
• 714957-48-9 1-(3-iodo-5-methyl-hexyl)-4-methoxy-benzene 
• 714957-49-0 4-[2-(4-methoxy-phenyl)-ethyl]-6-methyl-heptanoic acid ethyl ester 
• 714957-50-3 2-diazo-4-[2-(4-methoxy-phenyl)-ethyl]-6-methyl-heptanoic acid ethyl ester 

Relevant articles and documents

Cyclopentane construction by Rh-catalyzed intramolecular C-H insertion: Relative reactivity of a range of catalysts

The preparation and Rh-mediated cyclization of the α-diazoester 1 are outlined, and its utility in determining the elements that contribute to the reactivity of the intermediate Rh-carbenoid is presented. The rate of disappearance of diazo ester 1 catalyz

REDUCTION OF BENZYLIDENEACETONE DERIVATIVES WITH Pd/SiO2-AlPO4 AS CATALYST AND CYCLOHEXENE AS HYDROGEN DONOR

The hydrogen transfer reduction of benzylidenacetone derivatives p-X-C6H4-CH=CH-CO-R (X=-OCH3, H; R=C6H5, alkyl, OR, OH) using cyclohexene as hydrogen donor has been studied.The selective reduction of the C=C bond is observed and the effects of the nature of X and R, solvent, catalyst, and reaction temperature on the initial reaction rate are analyzed.In all cases, and for any substrate or catalyst, the reaction is firts-order with respect to the hydrogen donor and acceptor.