850254-51-2

Basic information

• Product Name: Benzene, 5-bromo-1,2-dimethoxy-3-(1-methylethyl)-
• CAS NO: 850254-51-2
• Molecular Formula: C11H15BrO2
• Molecular Weight: 259.143
• Mol File: 850254-51-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzene, 5-bromo-1,2-dimethoxy-3-(1-methylethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 5-bromo-1,2-dimethoxy-3-(1-methylethyl)-(850254-51-2)
• EPA Substance Registry System: Benzene, 5-bromo-1,2-dimethoxy-3-(1-methylethyl)-(850254-51-2)

Safety Data

• Hazardous Substances Data: 850254-51-2(Hazardous Substances Data)

Upstream product

• 181016-78-4 5-bromo-1-isopropenyl-2,3-dimethoxybenzene 
• 91-16-7 1,2-dimethoxybenzene 
• 857591-04-9 5-bromo-1-isopropyl-2-methoxy-3-nitrobenzene 
• 127293-44-1 4-bromo-2-isopropyl-6-nitrophenol 
• 181016-77-3 2‐(5‐bromo‐2,3‐dimethoxyphenyl)propan‐2‐ol 
• 153390-68-2 2-<2,3-dimethoxyphenyl>-propan-2-ol 
• 2150-42-7 methyl 2,3-dimethoxybenzoate 

Downstream Products

• 850254-61-4 4-[(E)-2-(3-Isopropyl-4,5-dimethoxy-phenyl)-vinyl]-3,3,4-trimethyl-cyclohexanone 
• 850254-59-0 3-[(E)-2-(3-Isopropyl-4,5-dimethoxy-phenyl)-vinyl]-3,4,4-trimethyl-6-oxo-cyclohex-1-enecarboxylic acid methyl ester 
• 850254-52-3 3-[2-(3-isopropyl-4,5-dimethoxy-phenyl)-2-methoxycarbonyloxy-ethyl]-3,4,4-trimethyl-6-oxo-cyclohex-1-enecarboxylic acid methyl ester 
• 850254-57-8 5-[2-(3-isopropyl-4,5-dimethoxy-phenyl)-2-methoxycarbonyloxy-ethyl]-4,4,5-trimethyl-2-oxo-cyclohexanecarboxylic acid methyl ester 
• 850254-56-7 4-[2-hydroxy-2-(3-isopropyl-4,5-dimethoxy-phenyl)-ethyl]-3,3,4-trimethyl-cyclohexanone 
• 1415689-45-0 1-isopropyl-2,3-dimethoxy-5-(methoxymethyl)benzene 
• 1415689-65-4 C₂₀H₂₀Cl₂FNO₅S 
• 1415689-49-4 methyl 4-isopropyl-2,3-dimethoxy-6-(methoxymethyl)benzoate 

Relevant articles and documents

Synthesis of [6,6,m]-Tricyclic Compounds via [4+2] Cycloaddition with Au or Cu Catalyst

We synthesized [6,6,6]- and [6,6,7]-tricyclic compounds via intramolecular [4+2] cycloaddition by gold or copper catalysts. Substrates for cyclization were prepared by coupling reactions between eight types of diyne and four types of aromatic moieties. We have successfully synthesized eleven tricyclic compounds.

The total synthesis of pygmaeocin C

Making use of a recently developed intramolecular Friedel-Crafts alkylation process as the key operation, the first total synthesis, in racemic form, of pygmaeocin C has been achieved. Georg Thieme Verlag Stuttgart.