83036-56-0

Basic information

• Product Name: Benzene, 1,2,3,4-tetramethoxy-5-methyl-6-(3-methyl-2-butenyl)-
• CAS NO: 83036-56-0
• Molecular Formula: C16H24O4
• Molecular Weight: 280.364
• Mol File: 83036-56-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzene, 1,2,3,4-tetramethoxy-5-methyl-6-(3-methyl-2-butenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,2,3,4-tetramethoxy-5-methyl-6-(3-methyl-2-butenyl)-(83036-56-0)
• EPA Substance Registry System: Benzene, 1,2,3,4-tetramethoxy-5-methyl-6-(3-methyl-2-butenyl)-(83036-56-0)

Safety Data

• Hazardous Substances Data: 83036-56-0(Hazardous Substances Data)

Upstream product

• 35896-58-3 2,3,4,5-tetramethoxytoluene 
• 556-82-1 3-methyl-2-buten-1-ol 
• 64135-15-5 diethyl (3-methylbut-2-en-1-yl) phosphate 
• 918800-77-8 2,3,4,5-tetramethoxy-6-methylphenylmagnesium bromide 
• 83036-58-2 prenyl diisopropyl phosphate 

Downstream Products

• 99347-66-7 [2-Chloro-1,1-dimethyl-3-(2,3,4,5-tetramethoxy-6-methyl-phenyl)-propylsulfanyl]-acetic acid methyl ester 
• 99347-55-4 [2-Chloro-2-methyl-1-(2,3,4,5-tetramethoxy-6-methyl-benzyl)-propylsulfanyl]-acetic acid methyl ester 
• 99347-75-8 [2-Methyl-1-(2,3,4,5-tetramethoxy-6-methyl-benzyl)-allylsulfanyl]-acetic acid methyl ester 
• 99347-98-5 (E)-4-Methyl-6-(2,3,4,5-tetramethoxy-6-methyl-phenyl)-hex-4-enoic acid methyl ester 
• 26539-07-1 4-methyl-6-(3-methyl-5,6-dimethoxy-1,4-benzoquinon-2-yl)hex-4-enoic acid 
• 94828-24-7 1,2,3,4-Tetramethoxy-5-methyl-6-(3-methyl-2-phenylsulfanyl-but-3-enyl)-benzene 
• 94828-31-6 methyl (E)-2-methyl-4-(2,3,4,5-tetramethoxy-6-methylphenyl)but-2-en-1-ol 
• 99347-82-7 1-(2-Chloro-3-methyl-but-3-enyl)-2,3,4,5-tetramethoxy-6-methyl-benzene 

Relevant articles and documents

Convenient syntheses of vitamin K and coenzyme Q by the coupling of Grignard reagents with allylic phosphate

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AN EFFICIENT REGIO- AND STEREOSPECIFIC ALKENYLATION OF PHENOLIC ETHERS BY PRENYL AND GERANYL DIISOPROPYL PHOSPHATES

Prenyl and geranyl diisopropyl phosphates readily alkenylate a variety of phenolic ethers regio- and stereospecifically without any appreciable side reactions.