54614-64-1

Basic information

• Product Name: 1-Butanone, 3-methyl-1-[2,4,6-trihydroxy-3-(3-methyl-2-butenyl)phenyl]-
• Synonyms: 3-Methyl-1-[2,4,6-trihydroxy-3-(3-methyl-but-2-enyl)-phenyl]-butan-1-on;1-Butanone,3-methyl-1-[2,4,6-trihydroxy-3-(3-methyl-2-butenyl)phenyl];3-methyl-1-[2,4,6-trihydroxy-3-(3-methyl-but-2-enyl)-phenyl]-butan-1-one;2',4',6'-trihydroxy-3'-(3-methylbut-2-enyl)isovalerophenone;{3-(3-methyl-2-butenyl)-2,4,6-trihydroxyphenyl} (2-methylpropyl) ketone
• CAS NO: 54614-64-1
• Molecular Formula: C16H22O4
• Molecular Weight: 278.34300
• Mol File: 54614-64-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-Butanone, 3-methyl-1-[2,4,6-trihydroxy-3-(3-methyl-2-butenyl)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Butanone, 3-methyl-1-[2,4,6-trihydroxy-3-(3-methyl-2-butenyl)phenyl]-(54614-64-1)
• EPA Substance Registry System: 1-Butanone, 3-methyl-1-[2,4,6-trihydroxy-3-(3-methyl-2-butenyl)phenyl]-(54614-64-1)

Safety Data

• Hazardous Substances Data: 54614-64-1(Hazardous Substances Data)

Usage

Uses

3-Methyl-1-[2,4,6-trihydroxy-3-(3-methyl-2-buten-1-yl)phenyl]-1-butanone is an impurity in the synthesis of Lupulone (L478000), a hop plant (Humulus lupulus L.) acid that inhibits tumorigenicity of hepatocellular carcinoma cells.

Upstream product

• 67-56-1 methanol 
• 26103-97-9 phloroisovalerophenone 
• 124-41-4 sodium methylate 
• 870-63-3 prenyl bromide 
• 358-72-5 dimethylallyl diphosphate 
• 108-73-6 3,5-dihydroxyphenol 
• 108-12-3 isopentanoyl chloride 

Downstream Products

• 93796-35-1 6-isopentyl-4-(3-methylbut-2-enyl)-3,5,6-trihydroxy-2-isovalerylcyclohexa-2,4-dien-1-one 
• 93796-34-0 2',4',6'-trihydroxy-3'-isopentyl-5'-(3-methylbut-2-enyl)isovalerophenone 
• 58461-24-8 4-isopentyl-6-(3-methylbut-2-enyl)-3,5,6-trihydroxy-2-isovalerylcyclohexa-2,4-dien-1-one 
• 26104-01-8 3-methyl-1-(2,4,6-trihydroxy-3-isopentylphenyl)butan-1-one 

Relevant articles and documents

gem-Diprenylation of Acylphloroglucinols by a Fungal Prenyltransferase of the Dimethylallyltryptophan Synthase Superfamily

Aspergillus terreus aromatic prenyltransferase (AtaPT) catalyzes predominantly C-monoprenylation of acylphloroglucinols in the presence of different prenyl diphosphates. With dimethylallyl diphosphate (DMAPP) as prenyl donor, gem-diprenylated products 1D3, 2D3, and 3D3 were also detected. High conversion of 1D1 to 1D3, 2D1 to 2D3, and 3D1 to 3D3 was demonstrated by incubation with AtaPT and DMAPP. The first example of gem-diprenylation by a member of the dimethylallyltryptophan synthase superfamily is provided.

Polyhydroxyphenol derivatives and preventive and therapeutic agents for bone and cartilage diseases containing the same

Compounds useful as preventive and therapeutic agents for bone and cartilage diseases; and drug compositions containing the same. The compounds are polyhydroxyphenol derivatives of general formula (I) and quinione analogues derived therefrom (wherein Rsu