70654-69-2

Basic information

• Product Name: 5-Bromo-2-(methoxymethoxy)-1,3-dimethylbenzene
• Synonyms: 5-Bromo-2-(methoxymethoxy)-1,3-dimethylbenzene
• CAS NO: 70654-69-2
• Molecular Formula: C₁₀H₁₃BrO₂
• Molecular Weight: 245.1130
• Mol File: 70654-69-2.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 286 °C at 760 mmHg
• Flash Point: 118.5 °C
• Appearance: /
• Density: 1.324 g/cm³
• Vapor Pressure: 0.00466mmHg at 25°C
• Refractive Index: 1.524
• CAS DataBase Reference: 5-Bromo-2-(methoxymethoxy)-1,3-dimethylbenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Bromo-2-(methoxymethoxy)-1,3-dimethylbenzene(70654-69-2)
• EPA Substance Registry System: 5-Bromo-2-(methoxymethoxy)-1,3-dimethylbenzene(70654-69-2)

Safety Data

• Hazardous Substances Data: 70654-69-2(Hazardous Substances Data)

Usage

General Description

5-Bromo-2-(methoxymethoxy)-1,3-dimethylbenzene is a chemical compound with the molecular formula C10H13BrO2. It is a derivative of benzene, featuring two methyl groups and a bromine atom. The presence of the methoxymethoxy group indicates a substituent attached to the benzene ring, which can impact the compound's reactivity and biological activity. This chemical may be used in organic synthesis or as a building block for the preparation of other compounds. 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 articles and documents

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.