≥96% 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.
| Sonrisas canónicas | C1=CC=C(C=C1)C2=CC=C(O2)C=O |
|---|---|
| IUPAC Name | 5-phenylfuran-2-carbaldehyde |
| InChIKey | BMJHNNPEPBZULA-UHFFFAOYSA-N |
| INCHI | 1S/C11H8O2/c12-8-10-6-7-11(13-10)9-4-2-1-3-5-9/h1-8H |
| Isómeros SMILES | C1=CC=C(C=C1)C2=CC=C(O2)C=O |
| WGK Alemania | 3 |
| Peso molecular | 172.18 |
| Reaxy-Rn | 120525 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=120525&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 | Organic oxygen compounds |
| Clase | Organooxygen compounds |
| Subclass | Carbonyl compounds |
| Intermediate Tree Nodes | Aldehydes |
| Direct Parent | Aryl-aldehydes |
| Alternative Parents | Benzene and substituted derivatives Heteroaromatic compounds Furans Oxacyclic compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Aryl-aldehyde - Benzenoid - Monocyclic benzene moiety - Heteroaromatic compound - Furan - Oxacycle - Organoheterocyclic compound - Organic oxide - Hydrocarbon derivative - Aromatic heteromonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as aryl-aldehydes. These are compounds containing an aldehyde group directly attached to an aromatic ring. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 G2431408 | Certificate of Analysis | May 09, 2026 | P119115 |
| G2431409 | Certificate of Analysis | May 09, 2026 | P119115 |
| K1827114 | Certificate of Analysis | Jan 27, 2026 | P119115 |
| K1827113 | Certificate of Analysis | Jan 26, 2026 | P119115 |
| C1411024 | Certificate of Analysis | Feb 22, 2022 | P119115 |
| Punto de inflamación (°F) | 230 °F |
|---|---|
| Punto de inflamación (°C) | 110°C |
| Punto de ebullición (°C) | 104-108°C |
| Punto de fusión (°C) | 29-33°C |
| Peso molecular | 172.180 g/mol |
| XLogP3 | 1.900 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 2 |
| Exact Mass | 172.052 Da |
| Monoisotopic Mass | 172.052 Da |
| Topological Polar Surface Area | 30.200 Ų |
| Heavy Atom Count | 13 |
| Formal Charge | 0 |
| Complexity | 173.000 |
| 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. Xiuquan Jia, Jiping Ma, Min Wang, Xiaofang Li, Jin Gao, Jie Xu. (2016) Alkali α-MnO2/NaxMnO2 collaboratively catalyzed ammoxidation–Pinner tandem reaction of aldehydes. Catalysis Science & Technology, 6 (20): (7429-7436). [PMID:] [10.1039/C6CY00874G] |
