15934-57-3

Basic information

• Product Name: 4-METHYL-3-PHENYLPENTAN-2-ONE, TECH
• Synonyms: 4-METHYL-3-PHENYLPENTAN-2-ONE, TECH
• CAS NO: 15934-57-3
• Molecular Formula: C₁₂H₁₆O
• Molecular Weight: 176.25484
• Mol File: 15934-57-3.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 115-118 °C(Press: 28 Torr)
• Appearance: /
• Density: 0.944±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 4-METHYL-3-PHENYLPENTAN-2-ONE, TECH(CAS DataBase Reference)
• NIST Chemistry Reference: 4-METHYL-3-PHENYLPENTAN-2-ONE, TECH(15934-57-3)
• EPA Substance Registry System: 4-METHYL-3-PHENYLPENTAN-2-ONE, TECH(15934-57-3)

Safety Data

• Hazardous Substances Data: 15934-57-3(Hazardous Substances Data)

Usage

Uses

4-Methyl-3-phenylpentan-2-one can be used for fungicidal activity.

Upstream product

• 873389-26-5 2,3-dimethyl-1-phenyl-butane-1,2-diol 
• 917-64-6 methyl magnesium iodide 
• 5558-29-2 3-methyl-2-phenyl-butyronitrile 
• 187737-37-7 propene 
• 2439-44-3 3-methyl-2-phenylbutanal 
• 74-88-4 methyl iodide 
• 103-79-7 1-phenyl-acetone 
• 57918-71-5 1-Phenyl-2-propanone Potassium Enolate 
• 5166-53-0 5-methyl-3-hexene-2-one 
• 1068-55-9 isopropylmagnesium chloride 
• 1901-26-4 3-methyl-4-phenyl-3-buten-2-one 
• 63866-06-8 1-Phenyl-2-propanone Dianion 
• 75-26-3 isopropyl bromide 
• 3815-34-7 2,2-dimethyl-1-phenyl-1,3-butanedione 

Downstream Products

• 1486516-51-1 (E)-3,5-dimethyl-4-phenylhex-2-en-1-ol 
• 108300-09-0 5-methyl-4-phenyl-1-piperidino-hexan-3-one; hydrochloride 
• 50870-06-9 1-Amino-3-methyl-2-naphthalenecarbonitrile 

Relevant articles and documents

Steric parameters in the Ir-catalyzed regio- and diastereoselective isomerization of primary allylic alcohols

The iridium-catalyzed diastereo- and regioselective isomerization of primary allylic alcohols using Crabtree's catalyst or sterically modified analogs is reported. The importance of the size of the substituents on either the substrates or the catalysts has been rationalized by linear free energy relationships.

Solid-Liquid Phase-Transfer Catalysis without Solvent: Selective Mono- and Di-alkylation of Benzyl Methyl Ketone

The alkylation of benzyl methyl ketone 1 has been performed by phase-transfer catalysis without solvent.Excellent yields of mono- 2 and di-alkyl derivatives 3 and 4 were obtained through general, selective and mild conditions.