30543-91-0

Basic information

• Product Name: Sesquichamaenol
• Synonyms: (±)-Sesquichamenol;Sesquichamaenol;Sesquichamenol;(S)-5-(2-Hydroxy-5-methylphenyl)-6-methyl-2-heptanone;2-[(S)-1-Isopropyl-4-oxopentyl]-4-methylphenol;Litseachromolaevane A
• CAS NO: 30543-91-0
• Molecular Formula: C₁₅H₂₂O₂
• Molecular Weight: 234.33
• Mol File: 30543-91-0.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Sesquichamaenol(CAS DataBase Reference)
• NIST Chemistry Reference: Sesquichamaenol(30543-91-0)
• EPA Substance Registry System: Sesquichamaenol(30543-91-0)

Safety Data

• Hazardous Substances Data: 30543-91-0(Hazardous Substances Data)

Upstream product

• 130633-10-2 5-hydroxy-5-(2'-methoxy-5'-methylphenyl)-6-methylheptan-2-one 
• 130633-08-8 1-(2'-methoxy-5'-methylphenyl)-2-methylpropan-1-ol 
• 7083-19-4 2-methoxy-5-methylbenzaldehyde 
• 73256-91-4 5-hydroxy-5-(2'-methoxy-5'-methylphenyl)-6-methylhept-1-ene 
• 30574-34-6 1-(2-methoxy-5-methyl phenyl)-2-methyl-propane-1-one 
• 613-84-3 2-hydroxy-5-methylbenzaldehyde 
• 162708-18-1 3,4-dihydro-1-(1-methylethyl)-7-methylnaphthalene 
• 162708-19-2 4-(1-methylethyl)-6-methyl-1,2,3,4-tetrahydronaphthalene 
• 83088-55-5 (+/-)-8-Hydroxy-2-methyl-8-isopropyl-5.6.7.8-tetrahydro-naphthalin 
• 22009-37-6 7-methyl-3,4-dihydro-2H-naphthalen-1-one 
• 228257-33-8 methyl 4-isopropyl-4-m-tolylbutyrate 
• 57494-10-7 3,4-dihydro-6-methyl-4-(1-methylethyl)-1(2H)-naphthalenone 
• 84498-31-7 3-dimethylamino-m-methylpropiophenone hydrochloride 
• 57494-18-5 4-isopropyl-4-m-tolyl-γ-butyrolactone 

Relevant articles and documents

The first total syntheses of the sesquiterpenes (±)-1,10;7,10- bisepoxy-1,10-seco-calamanene and (±)-6,7;7,10-bisepoxy-6,7-seco- calamanene

First total syntheses of the tricyclic sesquiterpenes mentioned in the title containing a benzo-fused 2,8-dioxabicyclo[3.2.1]octane framework, confirming the structures of the natural products, are described. Georg Thieme Verlag Stuttgart.

Biogenetic-type Synthesis of Sesquichamaenol

A hypothetical biosynthetic pathway for the conversion of farnesylpyrophosphate into seaquichamaenol 1, a modified sesquiterpenoid isolated from Chaemaecyparis formosensis Matsum is proposed. The synthesis of 1 which lends experimental support to the prop

Synthesis of phenolic sesquiterpenes via oxidative cleavage of benzocycloalkenols

Phenolic sesquiterpenes including sesquichamaenol, 6-(2-hydroxy-4-methylphenyl)-2-methyl-3-heptanone, and curcuphenol methyl ether have been obtained from oxidative cleavage of bicyclic precursors by treatment with acidic hydrogen peroxide in a process wh