1710-13-0

Basic information

• Product Name: 3,5-Furandicarboxylic acid dimethyl ester
• Synonyms: 2,4-Furandicarboxylic acid dimethyl ester;3,5-Furandicarboxylic acid dimethyl ester;Furan-2,4-dicarboxylic acid dimethyl ester
• CAS NO: 1710-13-0
• Molecular Formula: C₈H₈O₅
• Molecular Weight: 184.15
• Mol File: 1710-13-0.mol
• Article Data: 3

Chemical Properties

• Melting Point: 104-107 °C
• Boiling Point: 265.3±20.0 °C(Predicted)
• Appearance: /
• Density: 1.244±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 3,5-Furandicarboxylic acid dimethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-Furandicarboxylic acid dimethyl ester(1710-13-0)
• EPA Substance Registry System: 3,5-Furandicarboxylic acid dimethyl ester(1710-13-0)

Safety Data

• Hazardous Substances Data: 1710-13-0(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 20842-02-8 potassium furan-2-carboxylate 
• 498-60-2 furan-3-carboxaldehyde 
• 1170719-56-8 4-formyl-furan-2-carboxylic acid methyl ester 
• 186581-53-3 diazomethane 
• 1170719-57-9 furan-2,4-dicarboxylic acid 2-methyl ester 
• 98556-04-8 furan-2,3,5-tricarboxylic acid 
• 4282-28-4 2,4-furan dicarboxylic acid 

Downstream Products

• 197846-05-2 2-bromofuran-3-carboxylic acid 
• 98273-12-2 5-chlorocarbonyl-furan-3-carboxylic acid methyl ester 
• 102169-71-1 4-methoxycarbonyl-2-furaldehyde 
• 603999-19-5 5-formyl-furan-3-carboxylic acid 
• 21984-93-0 5-Methyl-furan-carbonsaeure-(3) 

Relevant articles and documents

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The scent of bacteria: Headspace analysis for the discovery of natural products

Volatile compounds released by 50 bacterial strains, 45 of them actinobacteria in addition to three chloroflexi and two myxobacteria, have been collected by use of a closed-loop stripping apparatus, and the obtained headspace extracts have been analyzed by GC-MS. Excluding terpenes that have recently been published elsewhere, 254 compounds from all kinds of compound classes have been identified. For unambiguous compound identification several reference compounds have been synthesized. Among the detected volatiles 12 new natural products have been found, in addition to mellein, which was released by Saccharopolyspora erythraea. The iterative PKS for this compound has recently been identified by in vitro experiments, but mellein production in S. erythraea has never been reported before. These examples demonstrate that headspace analysis is an important tool for the discovery of natural products that may be overlooked using conventional techniques. The method is also useful for feeding experiments with isotopically labeled precursors and was applied to investigate the biosynthesis of the unusual nitrogen compound 1-nitro-2-methylpropane, which arises from valine. Furthermore, several streptomycetes emitted compounds that were previously recognized as insect pheromones, thus questioning if bacterial symbionts are involved in insect communication.