30199-27-0

Basic information

• Product Name: (R)-2-methoxy-1-methyl-4-(6-methylhept-5-en-2-yl)benzene
• Synonyms: (R)-2-methoxy-1-methyl-4-(6-methylhept-5-en-2-yl)benzene
• CAS NO: 30199-27-0
• Molecular Weight: 232.366
• Mol File: 30199-27-0.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: (R)-2-methoxy-1-methyl-4-(6-methylhept-5-en-2-yl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-2-methoxy-1-methyl-4-(6-methylhept-5-en-2-yl)benzene(30199-27-0)
• EPA Substance Registry System: (R)-2-methoxy-1-methyl-4-(6-methylhept-5-en-2-yl)benzene(30199-27-0)

Safety Data

• Hazardous Substances Data: 30199-27-0(Hazardous Substances Data)

Upstream product

• 1374459-91-2 (R)-4-(3-methoxy-4-methylphenyl)pentanal 
• 24470-78-8 isopropyltriphenylphosphonium iodide 
• 1244612-55-2 1-(3-methoxy-4-methylphenyl)-5-methylhex-4-en-1-one 
• 16666-80-1 triphenylphosphonio-1-methylethanide 
• 1374459-90-1 (R)-methyl 4-(3-methoxy-4-methylphenyl)pentanoate 
• 1374459-74-1 (E)-4-(3-methoxy-4-methylphenyl)pent-3-enoic acid 
• 80693-18-1 C₁₁H₁₄O₂ 
• 220728-76-7 Acetic acid (S)-3-methoxymethoxy-2-(3-methoxy-4-methyl-phenyl)-propyl ester 
• 220728-49-4 (S)-2-methoxy-1-methyl-4-(1-(phenylsulfonyl)propan-2-yl)benzene 
• 220728-57-4 Acetic acid (S)-3-hydroxy-2-(3-methoxy-4-methyl-phenyl)-propyl ester 
• 220728-73-4 Acetic acid (R)-3-hydroxy-2-(3-methoxy-4-methyl-phenyl)-propyl ester 
• 220728-63-2 2-tert-butyl-5-(3-methoxy-4-methyl-phenyl)-4,5-dihydro-[1,3]dioxepine 
• 220728-66-5 (R)-3-Methoxymethoxy-2-(3-methoxy-4-methyl-phenyl)-propan-1-ol 
• 220728-77-8 2-Methoxy-1-methyl-4-((S)-1-methyl-2-phenylsulfanyl-ethyl)-benzene 

Downstream Products

• 923602-62-4 C₁₆H₂₆O₃ 
• 1026066-32-9 6-(3-methoxy-4-methyl-phenyl)-2-methyl-hept-2-enoyl chloride 
• 923602-64-6 C₁₈H₂₆O₃ 
• 923602-63-5 C₁₈H₂₈O₄ 
• 924888-75-5 6-(3-methoxy-4-methyl-phenyl)-2-methyl-hept-2-enoic acid ethyl ester 
• 59684-62-7 (R)-(-)-xanthorrhizol 

Relevant articles and documents

Xanthorrhizol, a new sesquiterpene from Curcuma xanthorrhiza

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Method for preparing chiral alkyl compound by catalyzing asymmetric hydrogenation reaction of olefin with iron complex catalyst

The invention discloses a method for preparing a chiral alkyl compound by catalyzing asymmetric hydrogenation reaction of olefin with an iron complex catalyst, which comprises the steps of by taking disubstituted olefin as shown in a formula I defined in

Preparation and use of enantioenriched 2-aryl-propylsulfonylbenzene derivatives as valuable building blocks for the enantioselective synthesis of bisabolane sesquiterpenes

We have demonstrated that different enantioenriched 2-arylpropylsufonylbenzene derivatives are very useful building blocks for the synthesis of aromatic bisabolane sesquiterpenes. Their preparation and the exploitation of their chemical reactivity have been comprehensively investigated. Accordingly, the naturally occurring bisabolane sesquiterpenes (-)-curcuphenol, (-)-xanthorrhizol, (+)-glandulone A, (+)-curcudiol, (+)-turmerone and (+)-curcudiol-10-one were synthesized in high enantiomeric purity. It is worth noting that the compounds (+)-curcudiol-10-one and (+)-glandulone A were prepared in enantioenriched form for the first time. Through the proposed synthetic approaches, we were able to confirm both chemical structures and the absolute configurations previously assigned to the two aforementioned sesquiterpenes.