51490-01-8

Basic information

• Product Name: 2-Bromo-1-(3,4,5-trimethoxy-phenyl)-ethanone
• Synonyms: 2-Bromo-1-(3,4,5-trimethoxy-phenyl)-ethanone;2-Bromo-3',4',5'-trimethoxyacetophenone;3,4,5-Trimethoxyphenacyl bromide;Bromomethyl 3,4,5-trimethoxyphenyl ketone
• CAS NO: 51490-01-8
• Molecular Formula: C₁₁H₁₃BrO₄
• Molecular Weight: 289.12
• Mol File: 51490-01-8.mol
• Article Data: 42

Chemical Properties

• Melting Point: 63-67℃
• Boiling Point: 350.7°C at 760 mmHg
• Flash Point: 165.9°C
• Appearance: /
• Density: 1.402
• Vapor Pressure: 4.31E-05mmHg at 25°C
• Refractive Index: 1.533
• CAS DataBase Reference: 2-Bromo-1-(3,4,5-trimethoxy-phenyl)-ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Bromo-1-(3,4,5-trimethoxy-phenyl)-ethanone(51490-01-8)
• EPA Substance Registry System: 2-Bromo-1-(3,4,5-trimethoxy-phenyl)-ethanone(51490-01-8)

Safety Data

• Hazardous Substances Data: 51490-01-8(Hazardous Substances Data)

Usage

General Description

2-Bromo-1-(3,4,5-trimethoxy-phenyl)-ethanone is a chemical compound with the molecular formula C11H13BrO4. It is a derivative of acetophenone and contains a bromine atom and three methoxy groups attached to a phenyl ring. 2-Bromo-1-(3,4,5-trimethoxy-phenyl)-ethanone is used mainly as an intermediate in the synthesis of pharmaceuticals and other organic compounds. It has also been studied for its potential pharmacological and anti-inflammatory properties. Additionally, it has been used in the field of organic chemistry as a reagent in various reactions due to its unique chemical structure. Overall, 2-Bromo-1-(3,4,5-trimethoxy-phenyl)-ethanone is a versatile compound with a range of potential applications in both the pharmaceutical and chemical industries.

InChI:InChI=1/C11H13BrO4/c1-14-9-4-7(8(13)6-12)5-10(15-2)11(9)16-3/h4-5H,6H2,1-3H3

Upstream product

• 1136-86-3 methyl (3,4,5-trimethoxyphenyl) ketone 
• 186581-53-3 diazomethane 
• 4521-61-3 3,4,5-Trimethoxybenzoyl chloride 
• 118-41-2 Eudesmic acid 
• 55363-58-1 (3,4,5-trimethoxyphenyl)(phenyl)methanone 
• 52215-12-0 pyrrolidone hydrotribromide 

Downstream Products

• 82100-67-2 S-(3,4,5-trimethoxyphenacylmercapto)-4,5-dihydroimidazole 
• 42755-95-3 diethyl (2-oxo-2-(3,4,5-trimethoxyphenyl)ethyl)phosphonate 
• 1026703-46-7 5-Methyl-1-[4-(3,4,5-trimethoxy-phenyl)-thiazol-2-yl]-1H-pyrazole-4-carboxylic acid ethyl ester 
• 180900-29-2 2-(3-Benzyloxy-4,5-dimethoxy-benzoyl)-4-oxo-4-(3,4,5-trimethoxy-phenyl)-butyric acid ethyl ester 
• 180900-30-5 2-(3,5-Bis-benzyloxy-4-methoxy-benzoyl)-4-oxo-4-(3,4,5-trimethoxy-phenyl)-butyric acid ethyl ester 
• 864378-36-9 (3-aminobenzofuran-2-yl)(3,4,5-trimethoxyphenyl)-methanone 
• 87428-53-3 3,4,5-trimethoxy-α-hydroxyacetophenone 
• 828921-10-4 (2S,4R)-4-Hydroxy-pyrrolidine-1,2-dicarboxylic acid 1-[2,2-dimethoxy-2-(3,4,5-trimethoxy-phenyl)-ethyl] ester 2-[2-oxo-2-(3,4,5-trimethoxy-phenyl)-ethyl] ester 
• 864378-35-8 3-amino-6-methyl-2-(3,4,5-trimethoxybenzoyl) benzothiophene 
• 917232-25-8 2-fluoro-1-(3,4,5-trimethoxyphenyl)ethan-1-one 
• 1027558-45-7 5-Methyl-1-[4-(3,4,5-trimethoxy-phenyl)-thiazol-2-yl]-1H-pyrazole-4-carboxylic acid 
• 79106-73-3 3-{1-[2-Hydroxy-2-(3,4,5-trimethoxy-phenyl)-ethyl]-piperidin-4-yl}-3,4-dihydro-quinazolin-2-yl-cyanamide 
• 191671-31-5 2-carboxymethylthio-3',4',5'-trimethoxyacetophenone 

Relevant articles and documents

New thiazole-2(3H)-thiones containing 4-(3,4,5-trimethoxyphenyl) moiety as anticancer agents

A new series of thiazole-2(3H)-thiones containing 4-(3,4,5-trimethoxyphenyl) moiety were synthesized as diaryl-heterocylic analogs of combretastatin A-4 with anticancer activity. The cytotoxicity evaluation of synthesized compounds against cancer cell lin

Antiproliferative Activity of Diarylnaphthofurans through Microtubule Destabilization

The present communication deals with pharmacophore designing based on “Fragment-Based Drug Discovery” approach. Two series of compounds were synthesized and evaluated against human cancer cell lines by sulforhodamine assay, target studies through tubulin

1,3,4-thiadiazine compound and application thereof

The invention relates to a 1,3,4-thiadiazine compound, and the chemical structure of the compound is shown as a formula (I). The provided compound has a remarkable inhibition effect on human cervicalcancer cells Hela and human colon cancer cells HCT116, a