39622-80-5

Basic information

• Product Name: 1,3-Benzenedicarboxylic acid, 2-broMo-, 1,3-diMethyl ester
• Synonyms: 1,3-Benzenedicarboxylic acid, 2-broMo-, 1,3-diMethyl ester;2-Bromoisophthalic acid dimethyl ester;Dimethyl 2-bromoisophthalate
• CAS NO: 39622-80-5
• Molecular Formula: C₁₀H₉BrO₄
• Molecular Weight: 273.08006
• Mol File: 39622-80-5.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 313.0±22.0 °C(Predicted)
• Appearance: /
• Density: 1.505±0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 1,3-Benzenedicarboxylic acid, 2-broMo-, 1,3-diMethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Benzenedicarboxylic acid, 2-broMo-, 1,3-diMethyl ester(39622-80-5)
• EPA Substance Registry System: 1,3-Benzenedicarboxylic acid, 2-broMo-, 1,3-diMethyl ester(39622-80-5)

Safety Data

• Hazardous Substances Data: 39622-80-5(Hazardous Substances Data)

Usage

General Description

1,3-Benzenedicarboxylic acid, 2-broMo-, 1,3-diMethyl ester is also known as bromophthalide or 2-bromoisophthalic acid, 1,3-dimethyl ester. It is an organic compound with the chemical formula C10H9BrO4. This chemical is used as an intermediate for pharmaceuticals and agrochemicals, as well as in the synthesis of other organic compounds. It is a white to off-white solid with a slight odor and is insoluble in water. The compound is primarily used in research and development and is not widely available for general use. Its primary applications include its use as a reagent in organic chemistry and as a starting material for the synthesis of more complex compounds.

Upstream product

• 22433-91-6 2-bromoisophthalic acid 
• 74-88-4 methyl iodide 
• 67-56-1 methanol 
• 151603-30-4 2-bromobenzene-1,3-dicarboxylic acid dichloride 
• 39622-79-2 2-aminoisophthalic acid 
• 576-22-7 2-Bromo-m-xylene 

Downstream Products

• 59346-22-4 2,6-bis(hydroxymethyl)bromobenzene 
• 22433-91-6 2-bromoisophthalic acid 
• 32081-22-4 5H,9H-Chino<3,2,1-de>acridin-5,9-dion 

Relevant articles and documents

Isolation of Hypervalent Group-16 Radicals and Their Application in Organic-Radical Batteries

Using a newly prepared tridentate ligand, we isolated hypervalent sulfur and selenium radicals for the first time and characterized their structures. X-ray crystallography, electron spin resonance spectroscopy, and density functional theory calculations r

A NEW TYPE OF ANTITUMOR COMPOUNDS: DERIVATIVES OF 7-PROPANAMIDE SUBSTITUTED BENZOXABOROLE

The present disclosure relates to derivatives of 7-propanamide substituted benzoxaborole and their preparation and use. The structural general formula of the derivatives is (formula).The derivatives are used for the preparation of a medicament for the pre

A Molecular Torsion Balance Study: A Nearby Anionic Group Exerts Little Influence on Hydrophobic Interactions between Nonpolar Surfaces

Polar groups have a solvent ordering effect on water and therefore may affect hydrophobic binding energies for nearby lipophilic surfaces. This would mean that determinations of excess surface free energy association energies require consideration of nearby polar functional groups. This paper reports results of a study to measure this possible effect. It was concluded from the models used here that an anionic polar group nearby a hydrophobic surface has little or no effect on the magnitude of hydrophobic association.