≥98%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Ethyl 3-furoate undergoes regioselective palladium(0)-catalyzed arylation reaction with aryl bromides.
Ethyl 3-furoate was used as starting reagent for the synthesis of ethyl 2,3-bis(trifluoromethyl)-7-oxabicyclo[2,2,1]hepta-2,5-diene-5-carboxylate and 4-(1-hydroxy-1-methyl-ethyl)-furan-2-sulfonamide.
| Pubchem Sid | 504754350 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504754350 |
| Canonical Smiles | CCOC(=O)C1=COC=C1 |
| IUPAC Name | ethyl furan-3-carboxylate |
| InChIKey | LOFDXZJSDVCYAS-UHFFFAOYSA-N |
| INCHI | 1S/C7H8O3/c1-2-10-7(8)6-3-4-9-5-6/h3-5H,2H2,1H3 |
| Isomeric SMILES | CCOC(=O)C1=COC=C1 |
| WGK Germany | 3 |
| Molecular Weight | 140.14 |
| Beilstein | 18(3/4)4052 |
| Reaxy-Rn | 112585 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=112585&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Class | Furans |
| Subclass | Furoic acid and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Furoic acid esters |
| Alternative Parents | Furan-3-carboxylic acid esters Heteroaromatic compounds Carboxylic acid esters Oxacyclic compounds Monocarboxylic acids and derivatives Organooxygen compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Furoic acid ester - Furan-3-carboxylic acid ester - Furan-3-carboxylic acid or derivatives - Heteroaromatic compound - Carboxylic acid ester - Oxacycle - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as furoic acid esters. These are ester derivatives of furoic acid. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 K2124541 | Certificate of Analysis | Sep 08, 2025 | E156334 |
| A2112170 | Certificate of Analysis | Nov 01, 2024 | E156334 |
| A2112169 | Certificate of Analysis | Nov 01, 2024 | E156334 |
| C2023031 | Certificate of Analysis | Jan 11, 2024 | E156334 |
| H1929060 | Certificate of Analysis | Jun 07, 2023 | E156334 |
| Sensitivity | Air Sensitive,Heat Sensitive |
|---|---|
| Refractive Index | 1.46 |
| Flash Point(°F) | 138.2 °F |
| Flash Point(°C) | 59 °C |
| Boil Point(°C) | 95 °C/35 mmHg |
| Molecular Weight | 140.140 g/mol |
| XLogP3 | 1.800 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 3 |
| Exact Mass | 140.047 Da |
| Monoisotopic Mass | 140.047 Da |
| Topological Polar Surface Area | 39.400 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 122.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Zhijiang Guo, Qiong Chen, Taibo Liang, Baoyuan Zhou, Suhua Huang, Xiufeng Cao, Xiuli Wang, Zaisong Ding, Jiangping Tu. (2023) Functionalized carbon nano-enabled plant ROS signal engineering for growth / defense balance. Nano Today, [PMID:] [10.1016/j.nantod.2023.102045] |
