100058-86-4

Basic information

• Product Name: 2-PROPENOIC ACID, 2-METHYL-3-(5-METHYL-2-FURANYL)-, ETHYL ESTER, (2E)-
• Synonyms: 2-PROPENOIC ACID, 2-METHYL-3-(5-METHYL-2-FURANYL)-, ETHYL ESTER, (2E)-;ETHYL 2-METHYL-3-(5-METHYL-2-FURYL)ACRYLATE
• CAS NO: 100058-86-4
• Molecular Formula: C₁₁H₁₄O₃
• Molecular Weight: 0
• Mol File: 100058-86-4.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 263°C at 760 mmHg
• Flash Point: 112.9°C
• Appearance: /
• Density: 1.065g/cm³
• Vapor Pressure: 0.0105mmHg at 25°C
• Refractive Index: 1.512
• CAS DataBase Reference: 2-PROPENOIC ACID, 2-METHYL-3-(5-METHYL-2-FURANYL)-, ETHYL ESTER, (2E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-PROPENOIC ACID, 2-METHYL-3-(5-METHYL-2-FURANYL)-, ETHYL ESTER, (2E)-(100058-86-4)
• EPA Substance Registry System: 2-PROPENOIC ACID, 2-METHYL-3-(5-METHYL-2-FURANYL)-, ETHYL ESTER, (2E)-(100058-86-4)

Safety Data

• Hazardous Substances Data: 100058-86-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H14O3/c1-4-13-11(12)8(2)7-10-6-5-9(3)14-10/h5-7H,4H2,1-3H3/b8-7+

Upstream product

• 620-02-0 5-Methylfurfural 
• 535-11-5 Ethyl 2-bromopropionate 
• 534-22-5 2-methylfuran 

Downstream Products

• 69978-24-1 2-methyl-3-(5-methyl-[2]furyl)-allyl alcohol 
• 3004-93-1 2-methyloctanoic acid 

Relevant articles and documents

Process for the preparation of fatty acids

The invention discloses a method for preparing fatty acid. The method comprises the following steps: providing a first reactant which is a furan compound containing an carbonyl group; providing a second reactant which is a compound containing a carboxyl group, an ester group or an anhydride group and can participate in a condensation reaction with the carbonyl group of the first reactant; allowingthe first reactant and the second reactant to participate in a first condensation reaction, and allowing a C=O bond of the carbonyl group of the first reactant to be connected with alpha carbon of the carbonyl group of the second reactant and to be converted into a C=C bond so as to form a condensation product; and carrying out a second-step reaction under hydrogen pressure in the presence of a co-catalytic system of a hydrogenation catalyst and Lewis acid, opening a furan ring of the condensation product, carrying out hydrodeoxygenation at the same time, removing all oxygen except for oxygenin the carboxyl group, and allowing a carbon chain to be saturated so as to obtain the fatty acid.