58106-25-5

Basic information

• Product Name: 1-BROM0-4-METHOXY-2 5-DIMETHYLBENZENE&
• Synonyms: 1-BROM0-4-METHOXY-2 5-DIMETHYLBENZENE&
• CAS NO: 58106-25-5
• Molecular Formula: C₉H₁₁BrO
• Molecular Weight: 215.089
• Product Categories: Ethers;Organic Building Blocks;Oxygen Compounds
• Mol File: 58106-25-5.mol
• Article Data: 5

Chemical Properties

• Melting Point: 34-38 °C(lit.)
• Boiling Point: 250°Cat760mmHg
• Flash Point: >110 °C
• Appearance: /
• Density: 1.326g/cm³
• Vapor Pressure: 0.0352mmHg at 25°C
• Refractive Index: 1.532
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 1-BROM0-4-METHOXY-2 5-DIMETHYLBENZENE&(CAS DataBase Reference)
• NIST Chemistry Reference: 1-BROM0-4-METHOXY-2 5-DIMETHYLBENZENE&(58106-25-5)
• EPA Substance Registry System: 1-BROM0-4-METHOXY-2 5-DIMETHYLBENZENE&(58106-25-5)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37
• WGK Germany: 3
• Hazardous Substances Data: 58106-25-5(Hazardous Substances Data)

Usage

General Description

1-Bromo-4-methoxy-2,5-dimethylbenzene is a chemical compound with the molecular formula C9H11BrO. It is commonly used as an intermediate in the synthesis of pharmaceuticals and organic compounds. This chemical is a colorless to light yellow liquid with a strong odor, and it is insoluble in water but soluble in organic solvents. It is primarily used in the production of pesticides, dyes, and perfumes. It is also known for its use in the synthesis of specialty polymers and as a reagent in organic chemistry reactions. The compound is considered to have low toxicity, but it may cause irritation to the skin and eyes upon contact.

InChI:InChI=1/C9H11BrO/c1-6-5-9(11-3)7(2)4-8(6)10/h4-5H,1-3H3

Upstream product

• 1706-11-2 2,5-Dimethyl-anisol 
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• 77-78-1 dimethyl sulfate 
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Downstream Products

• 154546-92-6 2-bromo-5-methoxyterephthalic acid 
• 108125-19-5 4-Methoxy-2,5-dimethyl-diphenyl-sulfid 
• 4962-28-1 2,5-dimethyl-4-methoxyphenol 
• 117174-70-6 4-methoxy-2,5-dimethylaniline 
• 108123-04-2 1-benzenesulfonyl-4-methoxy-2,5-dimethyl-benzene 
• 2493-72-3 4-benzenesulfonyl-2,5-dimethyl-phenol 
• 154546-96-0 2-hydroxy-5-methoxyterephthalic acid 
• 406479-16-1 dimethyl 2-(carbazol-9-yl)-5-(2-ethylhexyloxy)terephthalate 
• 406485-14-1 1,4-bis(hydroxymethyl)-5-(2-ethylhexyloxy)-2-(carbazol-9-yl)benzene 
• 406479-18-3 1,4-bis(chloromethyl)-5-(2-ethylhexyloxy)-2-(carbazol-9-yl)benzene 
• 406479-13-8 2-(carbazol-9-yl)-5-methoxyterephthalic acid 
• 406479-15-0 dimethyl-2-(carbazol-9-yl)-5-hydroxyterephthalate 
• 406479-14-9 dimethyl 2-(carbazol-9-yl)-5-methoxyterephthalate 
• 209625-32-1 2-ethylhexyloxy-5-(9-phenylanthracen-10-yl)-1,4-bis(bromomethyl)benzene 

Relevant articles and documents

Photocatalytic Selective Bromination of Electron-Rich Aromatic Compounds Using Microporous Organic Polymers with Visible Light

Pure organic, heterogeneous, metal-free, and visible light-active photocatalysts offer a more sustainable and environmentally friendly alternative to traditional metal-based catalysts. Here we report a series of microporous organic polymers containing photoactive conjugated organic semiconductor units as heterogeneous photocatalysts for a visible-light-promoted, highly selective bromination reaction of electron-rich aromatic compounds using HBr as a bromine source and molecular oxygen as a clean oxidant. Via a simple Friedel-Crafts alkylation reaction, the microporous organic polymers were obtained by cross-linking of organic semiconductor compounds with defined valence and conduction band positions. The utilization of the simply prepared porous polymer-based photocatalytic systems opens new opportunities toward a sustainable and efficient material design for catalysis.

Synthesis of soluble phenyl-substituted poly(p-phenylenevinylenes) with a low content of structural defects

The synthesis and characterization of two new soluble poly(p-phenylenevinylenes) (PPVs) are reported. The polymers are poly(2-(2′,5′-bis(octyloxy)benzene)-1,4-phenylenevinylene) (BOP-PPV) and poly(2-(2′,5′-bis(octyloxy)benzene)-5-methoxy-1,4-phenyleneviny

Halogenation using Quaternary Ammonium Polyhalides. Part 22. Selective Bromination of Aromatic Ethers with Benzyltrimethylammonium Tribromide

The reaction of aromatic ethers with a stoicheiometric amount of benzyltrimethylammonium tribromide in dichloromethane-methanol or acetic acid-ZnCl2 under mild conditions gave, selectively, mono-, di-, or tri-bromo-substituted aromatic ethers in quantitative yields.