≥99% 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.
Product Introduction
3,5-Difluorocinnamic acid has been used in the synthesis of “unnatural” flavonoids and stilbenes in Escherichia coli.
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 | Phenylpropanoids and polyketides |
| Classe | Cinnamic acids and derivatives |
| Subclass | Cinnamic acids |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Cinnamic acids |
| Alternative Parents | Styrenes Fluorobenzenes Aryl fluorides Monocarboxylic acids and derivatives Carboxylic acids Organofluorides Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Cinnamic acid - Styrene - Halobenzene - Fluorobenzene - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Organic oxygen compound - Organohalogen compound - Organofluoride - Organooxygen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as cinnamic acids. These are organic aromatic compounds containing a benzene and a carboxylic acid group forming 3-phenylprop-2-enoic 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 | Article |
|---|---|---|---|
 L2214434 | Certificate of Analysis | Sep 07, 2026 | T120766 |
| L2214435 | Certificate of Analysis | Sep 07, 2026 | T120766 |
| L2214437 | Certificate of Analysis | Sep 07, 2026 | T120766 |
| L2214438 | Certificate of Analysis | Sep 07, 2026 | T120766 |
| L2214443 | Certificate of Analysis | Sep 07, 2026 | T120766 |
| L2214566 | Certificate of Analysis | Sep 07, 2026 | T120766 |
| K2129151 | Certificate of Analysis | Sep 08, 2025 | T120766 |
| K2129152 | Certificate of Analysis | Sep 08, 2025 | T120766 |
| C1307067 | Certificate of Analysis | Nov 11, 2024 | T120766 |
| A2419670 | Certificate of Analysis | Nov 24, 2023 | T120766 |
| A2419671 | Certificate of Analysis | Nov 24, 2023 | T120766 |
| A2419672 | Certificate of Analysis | Nov 24, 2023 | T120766 |
| A2419673 | Certificate of Analysis | Nov 24, 2023 | T120766 |
| A2419674 | Certificate of Analysis | Nov 24, 2023 | T120766 |
| E2305935 | Certificate of Analysis | Oct 23, 2021 | T120766 |
| Solubilité | Soluble in methanol |
|---|---|
| Point de fusion (°C) | 204°C |
| Poids moléculaire | 184.140 g/mol |
| XLogP3 | 2.100 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 2 |
| Exact Mass | 184.034 Da |
| Monoisotopic Mass | 184.034 Da |
| Topological Polar Surface Area | 37.300 Ų |
| Heavy Atom Count | 13 |
| Formal Charge | 0 |
| Complexity | 206.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 1 |
| Covalently-Bonded Unit Count | 1 |
