17486-86-1

Basic information

• Product Name: Benzenepropanol, a-(2-phenylethyl)-
• CAS NO: 17486-86-1
• Molecular Formula: C17H20O
• Molecular Weight: 240.345
• Mol File: 17486-86-1.mol
• Article Data: 39

Chemical Properties

• CAS DataBase Reference: Benzenepropanol, a-(2-phenylethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenepropanol, a-(2-phenylethyl)-(17486-86-1)
• EPA Substance Registry System: Benzenepropanol, a-(2-phenylethyl)-(17486-86-1)

Safety Data

• Hazardous Substances Data: 17486-86-1(Hazardous Substances Data)

Upstream product

• 104-53-0 3-phenyl-propionaldehyde 
• 3277-89-2 phenethylmagnesium bromide 
• 538-58-9 1,5-diphenyl-1,4-pentadiene-3-one 
• 67-64-1 acetone 
• 7647-01-0 hydrogenchloride 
• 64-17-5 ethanol 
• 35225-79-7 dibenzylideneacetone 
• 5396-91-8 1,5-diphenyl-3-pentanone 
• 58681-16-6 7,7-bis-(phenylthio)bicyclo<4.1.0>heptane 
• 935662-20-7 (S,S^S)-1-chloro-3-phenylpropyl p-tolyl sulfoxide 
• 165904-22-3 4,4,5,5-tetramethyl-2-phenethyl-1,3,2-dioxaborolane 
• 100-51-6 benzyl alcohol 
• 67-56-1 methanol 
• 15814-30-9 1,5-diphenyl-penta-1,4-diyn-3-one 

Downstream Products

• 40939-59-1 pent-2-ene-1,5-diyldibenzene 
• 89113-44-0 1,5-diphenyl-3-bromopentane 
• 52772-41-5 (E)-pent-2-ene-1,5-diyldibenzene 
• 5396-91-8 1,5-diphenyl-3-pentanone 
• 791809-40-0 6-phenyl-4-(2-phenylethyl)hex-3-en-2-one 
• 791809-54-6 3,4-epoxy-6-phenyl-4-(2-phenylethyl)hexan-2-one 
• 791809-38-6 4-hydroxy-6-phenyl-4-(2-phenylethyl)hexan-2-one 
• 791809-67-1 3,4-epoxy-1,1-difluoro-2-methyl-6-phenyl-4-(2-phenylethyl)hex-1-ene 
• 1718-50-9 1,5-diphenylpentane 
• 54833-31-7 1,5-dicyclohexylpentane 
• 29766-50-5 N-(1-phenethyl-3-phenyl-propyl)amine 
• 1033079-94-5 C₂₀H₂₂F₃NO₂ 
• 17486-89-4 p-Toluolsulfonsaeure-(1,5-diphenyl-pentyl-3-ester) 
• 1333156-03-8 1,5-diphenylpentan-3-yl acrylate 

Relevant articles and documents

Titanocene(II)-promoted carbonyl cyclopropylidenation utilizing 1,1-dichlorocyclopropanes

A variety of alkylidenecyclopropanes bearing various substituents on their cyclopropane ring were obtained by the titanocene(II)-promoted reaction of 1,1-dichlorocyclopropane derivatives with carbonyl compounds including esters and lactones.

COMPOUND AND LUBRICANT COMPOSITION

PROBLEM TO BE SOLVED: To provide a novel compound and a lubricant composition. SOLUTION: There is provided a compound which has a carbon number in the range of 25 or more and 45 or less, contains carbon and hydrogen and may contain oxygen, contains one or more unsaturated bonds, has a chain hydrocarbon group constituting the main chain, has 1 or more and 5 or less branched groups, has a cyclic hydrocarbon group at at least one terminal of the main chain and has 1 or more and 2 or less cyclic hydrocarbon groups as the branched group. SELECTED DRAWING: None COPYRIGHT: (C)2020,JPOandINPIT

Hydrogenation of Ketones and Esters Catalyzed by Pd/C?SiO2

Hydrogenation of unsaturated ketones and esters with molecular hydrogen on the 5%Pd/C?SiO2 heterogeneous catalyst has been studied. The reaction direction and yield are determined by the starting compounds structure. Hydrogenation of unsaturated ketones containing phenyl group at the double carbon–carbon atom is accompanied by the reduction of the ketone group into the alcohol one. Hydrogenation of unsaturated esters is accompanied by transesterification.

Manganese-Catalyzed β-Alkylation of Secondary Alcohols with Primary Alcohols under Phosphine-Free Conditions

Manganese(I) complexes bearing a pyridyl-supported pyrazolyl-imidazolyl ligand efficiently catalyzed the direct β-alkylation of secondary alcohols with primary alcohols under phosphine-free conditions. The β-alkylated secondary alcohols were obtained in moderate to good yields with water formed as the byproduct through a borrowing hydrogen pathway. β-Alkylation of cholesterols was also effectively achieved. The present protocol provides a concise atom-economical method for C-C bond formation from primary and secondary alcohols.