6132-37-2

Basic information

• Product Name: Ethyl 5-broMo-2-furoate, 97+%
• Synonyms: Ethyl 5-broMo-2-furoate, 97+%;Ethyl 5-bromofuran-2-carboxylate;2-Furancarboxylic acid, 5-broMo-, ethyl ester;ethyl 5-broMo-2-furancarboxylate;Ethyl 5-broMo-2-furoate
• CAS NO: 6132-37-2
• Molecular Formula: C₇H₇BrO₃
• Molecular Weight: 219.03268
• Mol File: 6132-37-2.mol
• Article Data: 18

Chemical Properties

• Melting Point: 17 °C
• Boiling Point: 243.2°Cat760mmHg
• Flash Point: 100.9°C
• Appearance: /
• Density: 1.533g/cm³
• Vapor Pressure: 0.0325mmHg at 25°C
• Refractive Index: 1.509
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: Ethyl 5-broMo-2-furoate, 97+%(CAS DataBase Reference)
• NIST Chemistry Reference: Ethyl 5-broMo-2-furoate, 97+%(6132-37-2)
• EPA Substance Registry System: Ethyl 5-broMo-2-furoate, 97+%(6132-37-2)

Safety Data

• Hazardous Substances Data: 6132-37-2(Hazardous Substances Data)

Usage

General Description

Ethyl 5-bromo-2-furoate is a chemical compound with a purity of at least 97%. It is commonly used in the pharmaceutical and chemical industries as a reagent or intermediate in the synthesis of various organic compounds. This chemical is known for its versatile properties, including its ability to serve as a building block in the production of pharmaceutical drugs, agrochemicals, and other fine chemicals. It is also used in research and development processes to create new and innovative compounds with potential therapeutic or industrial applications. As a highly pure compound, ethyl 5-bromo-2-furoate is considered to be a valuable and reliable chemical for a wide range of applications.

InChI:InChI=1/C7H7BrO3/c1-2-10-7(9)5-3-4-6(8)11-5/h3-4H,2H2,1H3

Upstream product

• 585-70-6 5-bromo-furan-2-carboxylic acid 
• 64-17-5 ethanol 
• 26726-16-9 5-bromofuran-2-carbonyl chloride 
• 75-03-6 ethyl iodide 
• 88-14-2 2-furanoic acid 
• 1917-15-3 5-methylfuran-2-carboxylic acid 
• 614-99-3 Ethyl 2-furoate 

Downstream Products

• 18812-36-7 5-diphenylmethylene-2(5H)-furanone 
• 3199-50-6 1-(5-bromofuran-2-yl)ethanone 
• 89282-37-1 5-bromo-2-furylcarbohydrazide 
• 252357-14-5 5-allylfuran-2-carboxylic acid ethyl ester 
• 299203-59-1 ethyl 5-(4-cyanophenyl)-2-furancarboxylate 
• 60336-07-4 4-(4-methoxyphenyl)-1-furoic acid ethyl ester 
• 5965-53-7 diethyl 2-ketoglutarate 
• 115102-47-1 5-ethoxy-furan-2-carboxylic acid 
• 1041085-71-5 5-(2-pyridin-2-ylphenyl)furan-2-carboxylic acid ethyl ester 
• 614-99-3 Ethyl 2-furoate 
• 1087349-10-7 ethyl 5-(3-hydroxyphenyl)furan-2-carboxylate 
• 1027335-54-1 5-(2-(4-n-butyl-1H-1,2,3-triazol-1-yl)-3-methylphenyl)furan-2-carboxylic acid ethyl ester 
• 1132825-36-5 5-[2-methyl-5-(4-morpholin-4-yl-phenylcarbamoyl)-phenyl]-furan-2-carboxylic acid ethyl ester 
• 1034619-77-6 ethyl 5-(5-benzoyl-4-chloro-6-(methylthio)-pyrimidin-2-yl)furan-2-carboxylate 

Relevant articles and documents

NOVEL COMPOUND AND PHARMACEUTICAL COMPOSITION COMPRISING SAME

The present disclosure relates to a novel compound and a pharmaceutical composition comprising the same. The compound according to the present disclosure has effects for activating autophagy, and thus can be valuably used for preventing or treating diseas

Method for preparing 2,5-furandicarboxylic acid

The invention discloses a method for preparing 2,5-furandicarboxylic acid. The method comprises the following steps: preparing the 2,5-furandicarboxylic acid by sequentially performing four-step reaction namely bromination reaction, esterification reaction, carbonylation reaction and hydrolysis reaction on furan-2-carboxylic acid, wherein a compound as shown in Formula 3, a compound as shown in Formula 4 and a compound as shown in Formula 5 are obtained by the bromination reaction, the esterification reaction and the carbonylation reaction respectively. Compared with the prior art, the invention can effectively solve the problem of not high yield or severe reaction condition requirement by improving the key overall process flow of the preparation method and reaction conditions of each step. The structural formulae of the compound as shown in Formula 3, the compound as shown in Formula 4 and the compound as shown in Formula 5 are as shown in the specification respectively.

Regioselective oxidative Pd-catalysed coupling of alkylboronic acids with pyridin-2-yl-substituted heterocycles

A total of 19 alkylated heterocycles (thiophenes, benzothiophenes, pyrroles, furans) were prepared (36-99% yield) from the respective pyridin-2-yl-substituted precursors employing alkylboronic acids as the C-H alkylating reagents in an oxidative (Ag2