74866-17-4

Basic information

• Product Name: 1-BROMO-3,4-DIMETHOXY-2-METHYLBENZENE
• Synonyms: 1-BROMO-3,4-DIMETHOXY-2-METHYLBENZENE
• CAS NO: 74866-17-4
• Molecular Formula: C₉H₁₁BrO₂
• Molecular Weight: 231.09
• Mol File: 74866-17-4.mol
• Article Data: 16

Chemical Properties

• Melting Point: 59-60 °C(Solv: methanol (67-56-1))
• Boiling Point: 252.9±35.0 °C(Predicted)
• Appearance: /
• Density: 1.360±0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 1-BROMO-3,4-DIMETHOXY-2-METHYLBENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-BROMO-3,4-DIMETHOXY-2-METHYLBENZENE(74866-17-4)
• EPA Substance Registry System: 1-BROMO-3,4-DIMETHOXY-2-METHYLBENZENE(74866-17-4)

Safety Data

• Hazardous Substances Data: 74866-17-4(Hazardous Substances Data)

Usage

General Description

1-Bromo-3,4-dimethoxy-2-methylbenzene is a chemical compound commonly used in organic synthesis. It is a substituted aromatic compound that contains a bromine atom and three methoxy groups attached to a methylbenzene ring. 1-BROMO-3,4-DIMETHOXY-2-METHYLBENZENE is often used as a reagent in various chemical reactions, such as in the preparation of other organic compounds. It is also used in the pharmaceutical industry as a precursor for the synthesis of certain drugs. As with all chemical compounds, proper handling and storage of 1-bromo-3,4-dimethoxy-2-methylbenzene is necessary to ensure safety and prevent any adverse effects on health and the environment.

Upstream product

• 91-16-7 1,2-dimethoxybenzene 
• 74-88-4 methyl iodide 
• 86-51-1 2,3-dimethyoxybenzaldehyde 
• 4463-33-6 1,2-dimethoxy-3-methylbenzene 

Downstream Products

• 188412-54-6 1-Heptyl-3,4-dimethoxy-2-methyl-benzene 
• 201471-80-9 4-(3,4-Dimethoxy-2-methyl-phenyl)-butyric acid methyl ester 
• 253196-04-2 C₉H₁₁LiO₂ 
• 34316-15-9 chelerythrinium 
• 15575-49-2 6-acetonyldihydrochelerythrine 
• 1354688-30-4 C₁₂H₁₈O₃ 
• 1354688-29-1 C₁₄H₂₁NO₄ 
• 1354688-32-6 C₁₄H₁₉NO₆ 
• 1354688-31-5 C₁₄H₂₀O₄ 
• 4463-33-6 1,2-dimethoxy-3-methylbenzene 
• 5722-94-1 2-methyl-3,4-dimethoxybenzoic acid 
• 213971-18-7 4-[3,4-Dimethoxy-2-methylphenyl]-3-MethylbutanoicAcid 
• 51234-09-4 2-methyl-3,4-dimethoxybenzaldehyde 
• 40101-09-5 bis(6-bromo-2,3-dimethoxyphenyl)ethane 

Relevant articles and documents

Pd-Catalyzed Nazarov-Type Cyclization: Application in the Total Synthesis of β-Diasarone and Other Complex Cyclopentanoids

We describe the palladium-catalyzed Nazarov-type cyclization of easily accessible (hetero)arylallyl acetates to pentannulated (hetero)arenes. This method provides ready access to various types of bi-, tri-, tetra-, and pentacyclic cyclopentanoids under ne

Transition metals in organic synthesis, part 96. First total synthesis of streptoverticillin: Unambiguous confirmation of the absolute configuration

Using an iron-mediated construction of the carbazole framework, the first synthesis of streptoverticillin is described and the absolute configuration of the natural product is confirmed. The synthesis exploits a novel oxygen-mediated aromatization of tric

A direct palladium-catalyzed route to selectively substituted carbazoles through sequential C-C and C-N bond formation: Synthesis of carbazomycin A

The present paper offers a synthetically simple one-pot procedure for the catalytic preparation of the biologically interesting class of carbazoles. The new procedure is based on the combined catalysis of palladium and norbornene starting from o-substituted iodoarenes and N-sulfonylated or N-acetylated o-bromoanilines. A well-known member of this class, carbazomycin A, has been successfully prepared.