22794-95-2

Basic information

• Product Name: Benzene, 1-bromo-2,4-dimethoxy-3-methyl-
• Synonyms: Benzene,1-bromo-2,4-dimethoxy-3-methyl;4-Brom-2-methylresorcinol-dimethylether;1-bromo-2,4-dimethoxy-3-methyl-benzene;3-Brom-2,6-dimethoxy-toluol;2,6-dimethoxy-3-bromotoluene;3-bromo-2,6-dimethoxytoluene
• CAS NO: 22794-95-2
• Molecular Formula: C9H11BrO2
• Molecular Weight: 231.089
• Mol File: 22794-95-2.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 96°C/2.5mmHg(lit.)
• Density: 1.360±0.06 g/cm3(Predicted)
• Refractive Index: 1.5530 to 1.5570
• CAS DataBase Reference: Benzene, 1-bromo-2,4-dimethoxy-3-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-bromo-2,4-dimethoxy-3-methyl-(22794-95-2)
• EPA Substance Registry System: Benzene, 1-bromo-2,4-dimethoxy-3-methyl-(22794-95-2)

Safety Data

• Hazardous Substances Data: 22794-95-2(Hazardous Substances Data)

Usage

General Description

Benzene, 1-bromo-2,4-dimethoxy-3-methyl- is a chemical compound with the molecular formula C9H11BrO2. It is a brominated derivative of benzene, and its structure includes a bromine atom, two methoxy groups, and a methyl group attached to the benzene ring. Benzene, 1-bromo-2,4-dimethoxy-3-methyl- is commonly used as a reagent in organic synthesis and chemical research. It is important to handle this chemical with caution, as it is considered toxic and harmful if inhaled, ingested, or comes into contact with skin. Additionally, it is flammable and should be stored and used in a well-ventilated area with appropriate safety measures in place.

Upstream product

• 33662-58-7 methyl 2,4-dihydroxy-3-methylbenzoate 
• 5673-07-4 2,6-dimethoxytoluene 
• 608-25-3 2-methylbenzene-1,3-diol 

Downstream Products

• 20935-62-0 1,3-dimethoxy-2,4-dimethylbenzene 
• 60059-09-8 2,4,5-trimethoxy-3-methylbenzaldehyde 
• 61203-54-1 4-bromo-2,6-dimethoxy-benzoic acid 
• 90649-95-9 4-Chloro-2,6-dimethoxybenzoic acid 
• 90610-62-1 4-Nitro-2,6-dimethoxy-toluol 
• 90561-18-5 5-bromo-1,3-dimethoxy-2-methylbenzene 
• 90416-41-4 4-Chlor-2,6-dimethoxy-toluol 
• 78025-95-3 2,4-diamino-5-(3',5'-dimethoxy-4'-methylbenzyl)pyrimidine hydrochloride 
• 78025-94-2 4-cyano-2,6-dimethoxytoluene 
• 1011-27-4 3,5-dimethoxy-4-methylbenzaldehyde 
• 25576-97-0 2,3,6-trimethoxytoluene 
• 78025-93-1 3,5-dimethoxy-4-methylaniline 
• 1044872-60-7 (2-bromo-3,5-dimethoxy-4-methyl-phenyl)-carbamic acid tert-butyl ester 
• 1044872-65-2 6-amino-2,4-dimethoxy-3-morpholin-4-ylmethyl-benzamide 

Relevant articles and documents

TREATMENT OF DISEASES BY EPIGENETIC REGULATION

The present disclosure provides non-naturally occurring polyphenol compounds that inhibit the bromodomain and extra terminal domain (BET) proteins. The disclosed compositions and methods can be used for treatment and prevention of cancer, including NUT midline carcinoma, Burkitt's Lymphoma, Acute Myelogenous Leukemia, and Multiple Myeloma; autoimmune or inflammatory diseases or conditions, and sepsis.

COMPOUNDS FOR THE PREVENTION AND TREATMENT OF CARDIOVASCULAR DISEASES

The present disclosure relates to compounds, which are useful for regulating the expression of apolipoprotein A-I (ApoA-I), and their use for treatment and prevention of cardiovascular disease and related disease states, including cholesterol- or lipid-related disorders, such as, for example, atherosclerosis.

Efficient halogenation of aromatic systems using N-halosuccinimides in ionic liquids

A simple, rapid and highly regioselective green protocol has been developed for the halogenation of aromatic systems with N-halosuccinimides using room temperature ionic liquids (ILs) as novel and recyclable reaction media to produce the corresponding halogenated aromatic compounds in high to quantitative yields. N-Halosuccinimides show enhanced reactivity in ionic liquids thereby reducing the reaction times dramatically and improving the yields substantially.