96501-81-4

Basic information

• Product Name: Benzene, 2-methoxy-1,4-bis(1-methylethoxy)-
• CAS NO: 96501-81-4
• Molecular Formula: C13H20O3
• Molecular Weight: 224.3
• Mol File: 96501-81-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzene, 2-methoxy-1,4-bis(1-methylethoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 2-methoxy-1,4-bis(1-methylethoxy)-(96501-81-4)
• EPA Substance Registry System: Benzene, 2-methoxy-1,4-bis(1-methylethoxy)-(96501-81-4)

Safety Data

• Hazardous Substances Data: 96501-81-4(Hazardous Substances Data)

Upstream product

• 121-33-5 vanillin 
• 824-46-4 methoxyhydroquinone 
• 75-26-3 isopropyl bromide 

Downstream Products

• 865838-59-1 tert-butyl-[7-(3,6-diisopropoxy-2-methoxyphenyl)heptyloxy]dimethylsilane 
• 1033591-46-6 3-bromo-2,5-diisopropoxy-6-methoxybenzaldehyde 
• 1610888-07-7 (3S,4E,6S,7S,9S,11E,13E)-15-(3-bromo-2,5-diisopropoxy-6-methoxyphenyl)-3,7-bis[(tert-butyldimethylsilyl)oxy]-9-hydroxy-4,6,14-trimethylpentadeca-4,11,13-trienamide 
• 1610887-82-5 (E)-1-bromo-3-(3-iodo-2-methylallyl)-2,5-diisopropoxy-4-methoxybenzene 
• 1610887-81-4 1-bromo-2,5-diisopropoxy-4-methoxy-3-(prop-2-yne-1-yl)benzene 
• 1610887-80-3 [3-(3-bromo-2,5-diisopropoxy-6-methoxyphenyl)prop-1-yne-1-yl]trimethylsilane 
• 1610887-79-0 1-bromo-3-(chloromethyl)-2,5-diisopropoxy-4-methoxybenzene 
• 1610887-78-9 (3-bromo-2,5-diisopropoxy-6-methoxyphenyl)methanol 
• 1118756-71-0 C₂₉H₅₂O₅Si 
• 101923-87-9 2'-hydroxy-3,4',6,6'-tetraisopropyloxy-2,5'-dimethoxychalcone 
• 101923-89-1 2-(3,6-Diisopropoxy-2-methoxy-phenyl)-5,7-diisopropoxy-6-methoxy-chromen-4-one 
• 101909-95-9 2'-hydroxy-3,4',6-triisopropyloxy-2,3',6'-trimethoxychalcone 
• 101909-90-4 3',5,6',7-tetrahydroxy-2',6-dimethoxyflavone 
• 92519-91-0 viscidulin III 

Relevant articles and documents

Synthesis of a cytotoxic ansamycin hybrid

The synthesis of a new ansamycin macrolactam derivative that contains an ansa chain based on ansamitocin and an aromatic core related to geldanamycin is reported. The selective introduction of the cyclic carbamoyl group at C7 and C9 relies on a biotransformation using a mutant strain of S. hygroscopicus, the geldanamycin producer. The ansamycin hybrid forms atropisomers that differ in their antiproliferative activity toward cancer cells.

Synthetic studies on flavone derivatives. XIV. Synthesis of 2',4'-5'-trioxygenated flavones

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