84159-64-8

Basic information

• Product Name: 4-ethoxy-3-methoxybromoacetylbenzene
• Synonyms: 4-ethoxy-3-methoxybromoacetylbenzene
• CAS NO: 84159-64-8
• Molecular Weight: 273.126
• Mol File: 84159-64-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-ethoxy-3-methoxybromoacetylbenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 4-ethoxy-3-methoxybromoacetylbenzene(84159-64-8)
• EPA Substance Registry System: 4-ethoxy-3-methoxybromoacetylbenzene(84159-64-8)

Safety Data

• Hazardous Substances Data: 84159-64-8(Hazardous Substances Data)

Upstream product

• 53293-05-3 Ethyl p-ethoxy-m-methoxybenzoylacetate 
• 3535-36-2 4-ethoxy-3-methoxybenzoil chloride 
• 498-02-2 1-(3-methoxy-4-hydroxyphenyl)ethanone 
• 22317-29-9 1-(4-(benzyloxy)-3-methoxyphenyl)-2-(2-methoxyphenoxy)ethan-1-one 
• 1835-12-7 3-methoxy-4-benzyloxy-α-bromoacetophenone 
• 22317-34-6 β-hydroxy-α-(2-methoxyphenoxy)4-hydroxy-3-methoxypropiophenone 
• 7382-59-4 guaiacylglycerol-β-guaiacyl ether 
• 1835-11-6 4-benzyloxy-3-methoxyacetophenone 
• 75665-89-3 1-<(4-ethoxy-3-methoxy)phenyl>ethan-1-one 

Downstream Products

• 123202-53-9 1-(4-ethoxy-3-methoxyphenyl)-3-hydroxypropan-1-one 
• 1234363-56-4 1-(4-ethoxy-3-methoxyphenyl)prop-2-en-1-one 
• 177493-45-7 C₁₉H₂₂O₆ 
• 120-25-2 4-ethoxy-3-methoxybenzaldehyde 
• 103169-77-3 2,5-bis-(4-ethoxy-3-methoxy-phenyl)-furan-3-carboxylic acid ethyl ester 
• 102657-52-3 2,5-bis-(4-ethoxy-3-methoxy-phenyl)-furan-3-carboxylic acid 
• 102475-57-0 1,4-bis-(4-ethoxy-3-methoxy-phenyl)-butane-1,4-dione 
• 102662-92-0 2,5-bis-(4-ethoxy-3-methoxy-phenyl)-furan 
• 77891-30-6 1-(4-ethoxy-3-methoxyphenyl)-3-hydroxy-2-(2-methoxyphenoxy)propan-1-one 
• 98751-47-4 1-(4-ethoxy-3-methoxyphenyl)-2,3-dihydroxy-1-propanone 
• 102895-21-6 2-(4-ethoxy-3-methoxy-benzoyl)-4-(4-ethoxy-3-methoxy-phenyl)-4-oxo-butyric acid ethyl ester 
• 186255-41-4 1-(4-ethoxy-3-methoxyphenyl)-2-(2-methoxyphenoxy)ethanone 

Relevant articles and documents

Non-oxidative vanadium-catalyzed co bond cleavage: Application to degradation of lignin model compounds

(Chemical Equation Presented) New direction: Changes In the ligand structure divert the reactivity of vanadium (V) oxo complexes from alcohol oxidation to a novel non-oxidative C-O bond cleavage. Thus, highly functionalized aryl enones can be selectively generated from lignin model compounds by vanadium-catalyzed cleavage of the β-O-4 linkage (see scheme; N blue, O red).