≥95% 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Sonrisas canónicas | C1=CC(=C(C=C1C(=O)C=O)F)F.O |
|---|---|
| IUPAC Name | 2-(3,4-difluorophenyl)-2-oxoacetaldehyde;hydrate |
| InChIKey | FFYIMFMDGMXVOF-UHFFFAOYSA-N |
| INCHI | 1S/C8H4F2O2.H2O/c9-6-2-1-5(3-7(6)10)8(12)4-11;/h1-4H;1H2 |
| Isómeros SMILES | C1=CC(=C(C=C1C(=O)C=O)F)F.O |
| CAS alternativo | 79784-34-2 |
| PubChem CID | 2782289 |
| Peso molecular | 170.12（anhy） |
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 | Benzenoids |
| Clase | Benzene and substituted derivatives |
| Subclass | Phenylacetaldehydes |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Phenylacetaldehydes |
| Alternative Parents | Benzoyl derivatives Aryl ketones Fluorobenzenes Aryl fluorides Alpha ketoaldehydes Organofluorides Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Phenylacetaldehyde - Benzoyl - Aryl ketone - Fluorobenzene - Halobenzene - Aryl fluoride - Aryl halide - Alpha-ketoaldehyde - Ketone - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organic oxygen compound - Aldehyde - Organofluoride - Organooxygen compound - Aromatic homomonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as phenylacetaldehydes. These are compounds containing a phenylacetaldehyde moiety, which consists of a phenyl group substituted at the second position by an acetalydehyde. |
| 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 |
|---|---|---|---|
 H2421210 | Certificate of Analysis | May 09, 2024 | D186674 |
| H2421211 | Certificate of Analysis | May 09, 2024 | D186674 |
| H2421212 | Certificate of Analysis | May 09, 2024 | D186674 |
| H2421213 | Certificate of Analysis | May 09, 2024 | D186674 |
| H2421221 | Certificate of Analysis | May 09, 2024 | D186674 |
| H2421222 | Certificate of Analysis | May 09, 2024 | D186674 |
| Punto de fusión (°C) | 85°C - 90°C |
|---|---|
| Peso molecular | 188.130 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 2 |
| Exact Mass | 188.029 Da |
| Monoisotopic Mass | 188.029 Da |
| Topological Polar Surface Area | 35.100 Ų |
| Heavy Atom Count | 13 |
| Formal Charge | 0 |
| Complexity | 193.000 |
| 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 | 2 |
