58720-40-4

Basic information

• Product Name: 2-Butanone, 4-(2,3,6-trimethylphenyl)-
• Synonyms: 3-Butanone,1-(2,3,6-trimethylphenyl);2-Butanone,4-(2,3,6-trimethylphenyl);4-(2,3,6-Trimethylphenyl)-2-butanone;4-(2,3,6-trimethyl-phenyl)-butan-2-one
• CAS NO: 58720-40-4
• Molecular Formula: C13H18O
• Molecular Weight: 190.285
• Mol File: 58720-40-4.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 290.3±9.0 °C(Predicted)
• Density: 0.945±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 2-Butanone, 4-(2,3,6-trimethylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Butanone, 4-(2,3,6-trimethylphenyl)-(58720-40-4)
• EPA Substance Registry System: 2-Butanone, 4-(2,3,6-trimethylphenyl)-(58720-40-4)

Safety Data

• Hazardous Substances Data: 58720-40-4(Hazardous Substances Data)

Upstream product

• 79-77-6 (E)-β-ionone 
• 36340-49-5 5,6-epoxy-trans-β-ionone 
• 66248-64-4 5,8-Dimethyltetralone-p-toluenesulphonylhydrazone 
• 66248-66-6 2-(3'-Propanol-1')-3,6-dimethylbenzaldehyd 
• 66248-67-7 2-(3'-Propanol-1')-3,6-dimethylbenzyl-alkohol 
• 66248-69-9 3-(2',3',5'-Trimethylphenyl)propanal-1 
• 66248-68-8 3-(2',3',5'-Trimethylphenyl)propanol-1 
• 14108-89-5 5,8-dimethyl-1,2-tetrahydronaphthalene 
• 34341-29-2 2,3,6-trimethylbenzaldehyde 
• 76964-13-1 2-formyl-3,4-dihydro-5,8-dimethylnaphthalene 
• 124211-43-4 4-(2-Hydroxymethyl-3,6-dimethyl-phenyl)-butan-2-ol 
• 124211-42-3 4-(3,6-dimethyl-2-formylphenyl)butan-2-one 
• 30316-18-8 1,2-dihydro-3,5,8-trimethyl-naphthalene 
• 488-23-3 1,2,3,4-Tetramethylbenzene 

Downstream Products

• 124211-41-2 5-(2,3,6-trimethylphenyl)-3-methylpenta-1,4-dien-3-ol 
• 57461-21-9 (3E)-4-(2,3,6-trimethylphenyl)but-3-en-2-one 
• 34341-29-2 2,3,6-trimethylbenzaldehyde 
• 2529-36-4 2,3,6-trimethylbenzoic acid 
• 476-73-3 1,2,3,4-benzenetetracaboxylic acid 
• 124211-40-1 4-(2,3,6-trimethylphenyl)-3-bromobutan-2-one 
• 59700-21-9 methyl-3 (trimethyl-2,3,6 phenyl)-5 pentene-1 ol-3 

Relevant articles and documents

Selectivity in palladium catalyzed arylation: Synthetic application leading to aromatized ionone natural products

The selectivity in aromatic substitution vs conjugate addition during palladium catalyzed reactions has been controlled simply by changing the base. These reaction conditions have been applied to the syntheses of aromatized β-ionone natural products 1 and its dihydroderivatives 7.

SYNTHESIS OF 3-METHYL-5-(2,3,6-TRIMETHYLPHENYL)-1-PENTEN-3-OL, AN ALGAL SESQUITERPENE.

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