104157-20-2

Basic information

• Product Name: 1,2,4,5-tetrakis(bromomethyl)-3,6-dimethoxybenzene
• Synonyms: 1,2,4,5-tetrakis(bromomethyl)-3,6-dimethoxybenzene
• CAS NO: 104157-20-2
• Molecular Weight: 509.858
• Mol File: 104157-20-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,2,4,5-tetrakis(bromomethyl)-3,6-dimethoxybenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,4,5-tetrakis(bromomethyl)-3,6-dimethoxybenzene(104157-20-2)
• EPA Substance Registry System: 1,2,4,5-tetrakis(bromomethyl)-3,6-dimethoxybenzene(104157-20-2)

Safety Data

• Hazardous Substances Data: 104157-20-2(Hazardous Substances Data)

Upstream product

• 117574-75-1 1-(bromomethyl)-2,5-dimethoxy-3,4,6-trimethylbenzene 
• 4537-09-1 1,4-dimethoxy-2,3,5-trimethyl-benzene 
• 205862-10-8 2,3-bis(bromomethyl)-1,4-dimethoxy-5,6-dimethylbenzene 
• 13199-54-7 1,4-dimethoxy-2,3,5,6-tetramethylbenzene 
• 527-17-3 Duroquinone 
• 39021-83-5 3,6-dimethoxy-o-xylene 

Downstream Products

• 128844-25-7 N,N'-bis(2,5-di-tert-butylphenyl)-9,10-dimethoxy-1,2,3,4,5,6,7,8-octahydro-2,3,6,7-anthracenetetracarboxylic 2,3:6,7-diimide 
• 1185046-29-0 1,2,4,5-tetrahex-2-ynyl-3,6-dimethoxybenzene 
• 205862-12-0 C₅₂H₇₂N₆O₈ 
• 732970-43-3 C₄₂H₅₆N₆O₄ 
• 128844-24-6 N,N'-bis(4-tert-butylphenyl)-9,10-dimethoxy-1,2,3,4,5,6,7,8-octahydro-2,3,6,7-anthracenetetracarboxylic 2,3:6,7-diimide 

Relevant articles and documents

Hydrindacene-based acetylenic macrocycles with horizontally and vertically ordered functionality arrays

The macrocyclization of 2,6-diethynyl hydrindacenes (1) with functional groups at mutually perpendicular positions results in the formation of novel macrocycles which, as a result of the hindered rotation of the hydrindacene units, possess directionally persistent peripheral functionalities. The two hydrindacene units in the dimer macrocycle (2) have been shown to interact electronically through their respective butadiyne moieties, whereas the trimer macrocycle (3) demonstrates a moderate degree of geometrical flexibility as a result of the five-membered hydrindacene rings. In addition, these trimer macrocycles contain a central cavity suitably sized for the inclusion of various solvent molecules. These new macrocycles can be further modified by introducing π-conjugated side groups, such as styryl and thienyl groups, as well as by attaching a variety of peripheral ester groups. Copyright

Repetitive Diels-Alder Reactions for the Growth of Linear Polyacenequinoid Derivatives

Starting from 2,3,5,6-tetramethylidene-7-oxanorbornane, repetitive quinone Diels-Alder/oxidation reactions produced a series of epoxypolyacenequinones with up to eleven linearly annulated rings.Epoxide ring opening-oxidation gave polyacenequinones with se