117565-90-9

Basic information

• Product Name: BENZENEACETIC ACID, 2-BROMO-5-METHOXY-, METHYL ESTER
• Synonyms: BENZENEACETIC ACID, 2-BROMO-5-METHOXY-, METHYL ESTER;Methyl 2-(2-broMo-5-Methoxyphenyl)acetate
• CAS NO: 117565-90-9
• Molecular Formula: C₁₀H₁₁BrO₃
• Molecular Weight: 259.098
• Mol File: 117565-90-9.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 309.006 °C at 760 mmHg
• Flash Point: 140.682 °C
• Appearance: /
• Density: 1.42 g/cm³
• Storage Temp.: 2-8°C
• CAS DataBase Reference: BENZENEACETIC ACID, 2-BROMO-5-METHOXY-, METHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: BENZENEACETIC ACID, 2-BROMO-5-METHOXY-, METHYL ESTER(117565-90-9)
• EPA Substance Registry System: BENZENEACETIC ACID, 2-BROMO-5-METHOXY-, METHYL ESTER(117565-90-9)

Safety Data

• Hazardous Substances Data: 117565-90-9(Hazardous Substances Data)

Usage

General Description

Benzeneacetic acid, 2-bromo-5-methoxy-, methyl ester is a chemical compound that falls under the category of aromatic homomonocyclic compounds. Its molecular formula is C10H11BrO3 and it is a relatively complex compound which can be used in a variety of chemical reactions. This particular ester has a benzene ring, indicating the presence of alternating double and single bonds. Methyl esters are commonly produced by the reaction between a carboxylic acid and methanol in the presence of a catalyst. The bromo and methoxy groups attached to the benzene ring of the compound contribute to its overall reactivity. Its specific uses depend on its ability to engage in further chemical reactions, though exact applications can vary widely in the field of chemical research.

Upstream product

• 27387-23-1 5-methoxy-2-bromophenylacetonitrile 
• 19614-12-1 2-bromo-5-methoxybenzyl bromide 
• 27060-75-9 4-bromo-3-methylanisole 
• 1798-09-0 m-methoxyphenylacetic acid 
• 67-56-1 methanol 
• 86826-93-9 2-(2-bromo-5-methoxyphenyl)acetic acid 

Downstream Products

• 123312-26-5 2-(2-Bromo-5-methoxy-phenyl)-N-[2-(3-methoxy-phenyl)-1-methyl-ethyl]-acetamide 
• 1069115-19-0 methyl 2-(2-bromo-5-methoxyphenyl)-2-methylpropanoate 
• 1192487-16-3 methyl 2-(2'-bromo-5'-methoxyphenyl)hexanoate 
• 1224954-09-9 methyl 2-(5-methoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetate 

Relevant articles and documents

N-SUBSTITUTED TETRAHYDROTHIENOPYRIDINE DERIVATIVES AND USES THEREOF

A compound of Formula (I) is provided that has been shown to be useful for treating a disease caused by a viral infection: (I) wherein R1, R2, R3, A, L, m, n, p and q are as defined herein.

Role of ortho -substituents on rhodium-catalyzed asymmetric synthesis of β-lactones by intramolecular C-H insertions of aryldiazoacetates

A rhodium-catalyzed asymmetric synthesis of β-lactones via intramolecular C-H insertion into the ester group of aryldiazoacetates has been developed. The β-lactones were synthesized in high yields and with high levels of diastereo- and enantioselectivity.

Facile synthesis of 4,5,6a,7-tetrahydrodibenzo[de,g]chromene heterocycles and their transformation to phenanthrene alkaloids

Oxa-Pictet-Spengler cyclization and microwave-assisted C-H arylation have been implemented as key steps in the synthesis of new isochroman heterocycles containing a 4,5,6a,7-tetrahydrodibenzo[de,g]chromene motif. These isochromans may be easily transformed to phenanthrene alkaloids via acidic cleavage of the isochroman ring and standard synthetic manipulations thereafter. The route described is attractive in that it provides access to two biologically interesting scaffolds in simple and high yielding synthetic steps.