29113-63-1

Basic information

• Product Name: ETHYL 2,5-DIMETHYL-3-FUROATE
• Synonyms: ETHYL 2,5-DIMETHYL-3-FUROATE;ETHYL 2,5-DIMETHYL-FURAN-3-CARBOXYLATE
• CAS NO: 29113-63-1
• Molecular Formula: C₉H₁₂O₃
• Molecular Weight: 168.19
• Mol File: 29113-63-1.mol
• Article Data: 21

Chemical Properties

• Boiling Point: 257.12°C (rough estimate)
• Flash Point: 83°C
• Appearance: /
• Density: 1.0478
• Vapor Pressure: 0.213mmHg at 25°C
• Refractive Index: 1.4686 (estimate)
• CAS DataBase Reference: ETHYL 2,5-DIMETHYL-3-FUROATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL 2,5-DIMETHYL-3-FUROATE(29113-63-1)
• EPA Substance Registry System: ETHYL 2,5-DIMETHYL-3-FUROATE(29113-63-1)

Safety Data

• Hazardous Substances Data: 29113-63-1(Hazardous Substances Data)

Usage

Synthesis Reference(s)

Tetrahedron Letters, 29, p. 4987, 1988 DOI: 10.1016/S0040-4039(00)80660-7

InChI:InChI=1/C9H12O3/c1-4-11-9(10)8-5-6(2)12-7(8)3/h5H,4H2,1-3H3

Upstream product

• 1117-96-0 Diazoethan 
• 636-44-2 2,5-dimethylfuran-3-carboxylic acid 
• 82537-43-7 4-(carboethoxy)-5-methylfuran-2-acetic acid 
• 41892-81-3 ethyl 2-acetyl-4-oxopentanoate 
• 1007476-32-5 sodium ethyl acetylacetate enolate 
• 78-95-5 chloroacetone 
• 625-86-5 2,5-dimethylfuran 
• 78582-65-7 trans ethyl 5-cyano-2,5-dimethyl-2,5-dihydrofuran-2-carboxylate 
• 78582-65-7 cis ethyl 5-cyano-2,5-dimethyl-2,5-dihydrofuran-2-carboxylate 
• 623-49-4 ethyl cyanoformate 
• 141-97-9 ethyl acetoacetate 
• 106-96-7 propargyl bromide 
• 122132-58-5 ethyl 2-methyl-5-methylene-4,5-dihydrofuran-3-carboxylate 
• 78582-65-7 ethyl 5-cyano-2,5-dimethyl-2,5-dihydrofuran-2-carboxylate 

Downstream Products

• 159881-93-3 2,5-dimethyl-furan-3-carboxylic acid hydrazide 
• 887576-69-4 4-iodo-2,5-dimethyl-furan-3-carboxylic acid ethyl ester 
• 1003-96-9 2,5-dimethyl-3-(hydroxymethyl)furan 
• 154160-55-1 (2,5-Dimethyl-3-furyl)methyl benzoate 
• 67243-00-9 2,5-dimethyl-[3]furylamine 
• 758724-17-3 (+/-)-2,5-dimethyl-4-(2-nitro-phenyl)-furan-3-carboxylic acid 
• 758724-21-9 (+/-)-2,5-dimethyl-4-(2-methyl-6-nitro-phenyl)-furan-3-carboxylic acid 
• 758725-23-4 (+/-)-4-(2,4-dimethyl-6-nitro-phenyl)-2,5-dimethyl-furan-3-carboxylic acid 
• 636-44-2 2,5-dimethylfuran-3-carboxylic acid 
• 28562-70-1 2,5-dimethyl-furan-3-carboxanilide 
• 865376-68-7 2,5-dimethyl-4-(2-methoxyphenyl)furan-3-carboxylic acid ethyl ester 
• 108123-02-0 2,5-dimethyl-4-phenylfuran-3-carboxylic acid ethyl ester 

Relevant articles and documents

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Preparation of polysubstituted dihydrofurans through a PhI(OAc)2-promoted haloenolcyclization of olefinic dicarbonyl compounds

A metal-free cyclization of olefinic dicarbonyl compounds for the synthesis of various 5-halomethyl-4,5-dihydrofurans is presented. Using (diacetoxyiodo)benzene as the reaction promoter and halotrimethylsilane as the halogen source, the intramolecular hal

Design, synthesis and antifungal activity of novel furancarboxamide derivatives

Twenty-seven novel furancarboxamide derivatives with a diphenyl ether moiety were synthesized and evaluated for their antifungal activity against Rhizoctonia solani, Botrytis cirerea, Valsa Mali and Sphaceloma ampelimum. Antifungal bioassay results indicated that most compounds had good or excellent fungicidal activities for R. solani and S. ampelimum at 20 mg L-1. Among synthesized compounds, compound 18e showed a greater inhibitory effect against S. ampelimum, with half maximal effective concentration (EC50) values of 0.020 mg L-1. This strong activity rivals currently used commercial fungicides, such as Boscalid and Carbendazim, and has great potential as a lead compound for future development of novel fungicides.