32365-53-0

Basic information

• Product Name: ethyl 5-formylfuran-3-carboxylate
• Synonyms: ethyl 5-formylfuran-3-carboxylate
• CAS NO: 32365-53-0
• Molecular Formula: C₈H₈O₄
• Molecular Weight: 168.14672
• Mol File: 32365-53-0.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 280.375°C at 760 mmHg
• Flash Point: 123.366°C
• Appearance: /
• Density: 1.216g/cm³
• Vapor Pressure: 0.004mmHg at 25°C
• Refractive Index: 1.515
• CAS DataBase Reference: ethyl 5-formylfuran-3-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 5-formylfuran-3-carboxylate(32365-53-0)
• EPA Substance Registry System: ethyl 5-formylfuran-3-carboxylate(32365-53-0)

Safety Data

• Hazardous Substances Data: 32365-53-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C8H8O4/c1-2-11-8(10)6-3-7(4-9)12-5-6/h3-5H,2H2,1H3

Upstream product

• 614-98-2 ethyl 3-furancarboxylate 
• 68-12-2 N,N-dimethyl-formamide 
• 216394-88-6 5-Dibromomethyl-furan-3-carboxylic acid ethyl ester 
• 121-45-9 phosphorous acid trimethyl ester 
• 26501-83-7 5-methyl-furan-3-carboxylic acid ethyl ester 
• 13129-23-2 methyl furan-3-carboxylate 
• 1311291-11-8 4-(ethoxycarbonyl)furan-2-carboxylic acid 
• 32365-49-4 5-hydroxymethyl-3-furancarboxylic acid ethyl ester 

Downstream Products

• 1314217-84-9 ethyl 5-{[(4-trifluoromethoxybenzyl)amino]methyl}-furan-3-carboxylate hydrochloride 
• 1314217-86-1 ethyl 7-methyl-1-oxo-2-[4-(trifluoromethoxy)benzyl]-2,3-dihydro-1H-isoindole-5-carboxylate 
• 1314358-28-5 ethyl 5-{[(4-trifluoromethoxybenzyl)amino]methyl}-furan-3-carboxylate 
• 1374160-80-1 C₂₀H₂₀F₃NO₅ 

Relevant articles and documents

HETEROARYLCARBOXYLIC ACID ESTER DERIVATIVE

The present invention provides a hyperglycemic inhibitor having a serine protease inhibitory action, which is a novel prophylactic or therapeutic drug for diabetes. A compound represented by the following formula (I), wherein each symbol is as defined in the description, or a pharmaceutically acceptable salt thereof

PROCESS FOR MAKING A METABOTROPIC GLUTAMATE RECEPTOR POSITIVE ALLOSTERIC MODULATOR - 874

Processes for making 7-methyl-5-(3piperazin-1-ylmethyl-[1,2,4]oxadiazol-5-yl)-2-(4- trifluoromethoxybenzyl)-2,3-dihydroisoindol-1-one

Intra-molecular Diels-Alder reactions of citraconamic acids from furfurylamines and citraconic anhydride: Effects of substitution in the furan ring on regioselectivity

Regioselectivity in the intra-molecular Diels-Alder (IMDA) reaction of furfurylcitraconamic acids derived from N-benzylfurfurylamines and citraconic anhydride can be controlled by substituents located in the furan ring and by reaction conditions. Reactions conducted under kinetic conditions resulted in cycloaddition products having methyl and aminomethylene substituent in 1,3-relationship whereas under thermodynamic conditions, excepting in the case of the 3-methylsulfanyl group, the products rearranged to more stable cycloadducts in which the substituents are in 1,2-relationship. Product formation can be explained on the basis of frontier orbital interactions and steric considerations.