70654-69-2

Usage

Uses

Used in Organic Synthesis:
5-Bromo-2-(methoxymethoxy)-1,3-dimethylbenzene is used as a building block in organic synthesis for the preparation of other compounds. Its unique structure and functional groups make it a valuable intermediate in the synthesis of various organic molecules.
Used in Pharmaceutical Industry:
5-Bromo-2-(methoxymethoxy)-1,3-dimethylbenzene is used as a starting material or intermediate in the development of pharmaceutical compounds. Its specific functional groups and reactivity can be utilized to create new drugs with potential therapeutic applications.
Used in Chemical Research:
5-Bromo-2-(methoxymethoxy)-1,3-dimethylbenzene is used as a research compound to study its properties, reactivity, and potential applications. Chemists and researchers can use 5-Bromo-2-(methoxymethoxy)-1,3-dimethylbenzene to explore new reaction pathways and develop innovative synthetic methods.
It is important for researchers and chemists to carefully handle and study the properties of 5-Bromo-2-(methoxymethoxy)-1,3-dimethylbenzene to better understand its potential applications and potential hazards.

InChI:InChI=1/C10H13BrO2/c1-7-4-9(11)5-8(2)10(7)13-6-12-3/h4-5H,6H2,1-3H3

Upstream product

• 109-87-5 Dimethoxymethane 
• 2374-05-2 4-bromo-2,6-dimethyl-phenol 

Downstream Products

• 906623-26-5 4-[4-(methoxymethoxy)-3,5-dimethylphenyl]pyridine 
• 144426-58-4 2,6-dimethyl-4-(pyridin-4'-yl)phenol 
• 223127-02-4 methyl 4'-methoxymethoxy-3',5'-dimethylbiphenyl-4-carboxylate 

Relevant academic research and scientific papers

Syntheses of sterically hindered pyridinium phenoxides as model compounds in nonlinear optics

Noncentrosymmetric molecules with a π-conjugated system and, among them, push-pull molecules such as pyridinium phenoxide, are a promising new class of materials for applications in optoelectronics due to their nonlinear optical (NLO) properties. Modelling studies have indicated that an increase in the twist angle between the two aromatic rings leads to an enhancement of the NLO properties. In order to confirm this feature experimentally, it was necessary to prepare a series of new hindered pyridinium phenoxides. Their efficient syntheses by Suzuki cross-coupling reactions are described herein. Wiley-VCH Verlag GmbH & Co. KGaA, 2006.

Novel synthesis of 3,3-substituted dihydrobenzisothiazole-1,1-dioxides and -2,3-dihydronaphtho-1,2-thiazine-1,1-dioxides

This invention relates to a method of synthesizing certain 3-(carbocyclic aryl)-3-(4'-OP-carbocyclic aryl)-2,3-dihydrobenz[d]isothiazole-1,1-dioxides (and -2,3-dihydronaphtho[1,8-de]-1,2-thiazine-1,1-dioxides) by reacting (a) a 4-OP-carbocyclic aryllithium compound wherein P is a protecting group and (b) a 3-(carbocyclic aryl)benz[d]isothiazole-1,1-dioxide wherein said 3-(carbocyclic aryl) moiety is other than a 3-(4'-OP-carbocyclic aryl) moiety to give (c) the corresponding 3-carbocyclic aryl)-3-(4'-OP-carbocyclic aryl)-2,3-dihydrobenz[d]isothiazole-1,1-dioxide. The -2,3-dihydronaphtho[1,8-de]-1,2-thiazine-1,1-dioxides are prepared in the same manner by reacting a 3-(carbocyclic aryl)naphtho[1,8-de]-1,2-thiazine-1,1-dioxide with said 4'-OP-carbocyclic aryllithium compound. In a further embodiment, the compounds synthesized according to the foregoing method are reacted with a carboxylic acid halide to give the corresponding 2-carbonyl-substituted 2,3-dihydrobenz[d]isothiazole-1,1-dioxide (or -2,3-dihydronaphtho[1,8-de]-1,2-thiazine-1,1-dioxides) followed by removing the protecting group, P, with weak acid to yield certain phenol and 1-naphthol sulfam(na)phthaleins useful, e.g., as optical filter agents and filter agent precursors in photography.