97088-24-9

Basic information

• Product Name: 1,4-dibromo-2,5-bis(methoxymethoxy)benzene
• Synonyms: 1,4-dibromo-2,5-bis(methoxymethoxy)benzene
• CAS NO: 97088-24-9
• Molecular Weight: 356.011
• Mol File: 97088-24-9.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1,4-dibromo-2,5-bis(methoxymethoxy)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-dibromo-2,5-bis(methoxymethoxy)benzene(97088-24-9)
• EPA Substance Registry System: 1,4-dibromo-2,5-bis(methoxymethoxy)benzene(97088-24-9)

Safety Data

• Hazardous Substances Data: 97088-24-9(Hazardous Substances Data)

Upstream product

• 109-87-5 Dimethoxymethane 
• 14753-51-6 2,5-dibromohydroquinone 
• 107-30-2 chloromethyl methyl ether 
• 123-31-9 hydroquinone 

Relevant articles and documents

Fluoride-Ion-Catalyzed Synthesis of Ladder-type Conjugated Benzobisbenzofurans via Intramolecular Nucleophilic Aromatic Substitution Reaction under Metal-free and Mild Conditions

The fluoride-ion-catalyzed synthesis of benzobisbenzofuran derivatives is described. Fluorine-containing aryl silyl ethers were reacted with 5 mol % of Bu4NF to give desired compounds in high yield under mild conditions. Syn-selective cyclizati

Et2SBr.SbCl5Br: An effective reagent for direct bromonium-induced polyene cyclizations

It's all about reactivity: Although bromonium-induced cation-π cyclizations are commonly utilized by nature to fashion six-membered rings from a diverse set of polyene precursors, no general laboratory method exists that can achieve the same breadth of substrate scope. An easily synthesized and handled reagent is described (see scheme) that is capable of directly, broadly, and rapidly effecting such reactions in good yield with a variety of geraniol, farnesol, and nerol derivatives.

The preparations and some properties of mixed aryl-thienyl oligomers and polymers

The syntheses by transition metal coupling reactions of a large number of oligomers constructed from benzene and thiophene rings are described. The first use of arylcadmium chlorides for such coupling reactions is reported. The routes chosen allow for rational variation in the modes of linkage, the substitution and the proportions of the two units. The benzene and thiophene rings are always joined in a known order and may bear a wide variety of regularly spaced functional groups. Additionally the shape of the oligomers may be varied at will. In all cases p-type doping with iodine or ferric chloride leads to large enhancements in conductivity.