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≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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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.
trans|-4-(Diethylamino)cinnamaldehyde is a potential building block to synthesis of longer wavelength Styryl dyes. Styryl dyes are commonly used as fluorescent compounds utilized in neurobiology research studies.
| Pubchem Sid | 504763792 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504763792 |
| Canonical Smiles | CCN(CC)C1=CC=C(C=C1)C=CC=O |
| IUPAC Name | (E)-3-[4-(diethylamino)phenyl]prop-2-enal |
| InChIKey | JXXOTBSUZDDHLT-AATRIKPKSA-N |
| INCHI | 1S/C13H17NO/c1-3-14(4-2)13-9-7-12(8-10-13)6-5-11-15/h5-11H,3-4H2,1-2H3/b6-5+ |
| Isomeric SMILES | CCN(CC)C1=CC=C(C=C1)/C=C/C=O |
| WGK Germany | 3 |
| PubChem CID | 5375106 |
| Molecular Weight | 203.28 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Phenylpropanoids and polyketides |
| Class | Cinnamaldehydes |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Cinnamaldehydes |
| Alternative Parents | Styrenes Dialkylarylamines Aniline and substituted anilines Enals Organopnictogen compounds Organic oxides Hydrocarbon derivatives Aldehydes |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Cinnamaldehyde - Styrene - Tertiary aliphatic/aromatic amine - Dialkylarylamine - Aniline or substituted anilines - Benzenoid - Monocyclic benzene moiety - Alpha,beta-unsaturated aldehyde - Enal - Tertiary amine - Amine - Aldehyde - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as cinnamaldehydes. These are organic aromatic compounds containing a cinnamlaldehyde moiety, consisting of a benzene and an aldehyde group to form 3-phenylprop-2-enal. |
| 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 |
|---|---|---|---|
| Certificate of Analysis | Mar 14, 2024 | T347020 | |
| Certificate of Analysis | Mar 14, 2024 | T347020 | |
| Certificate of Analysis | Mar 14, 2024 | T347020 | |
| Certificate of Analysis | Mar 14, 2024 | T347020 |
| Solubility | Soluble in water (partly). |
|---|---|
| Refractive Index | n20D1.58 (Predicted) |
| Boil Point(°C) | 355.40° C at 760 mmHg (Predicted) |
| Melt Point(°C) | 74-76° C (lit.) |
| Molecular Weight | 203.280 g/mol |
| XLogP3 | 3.100 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 5 |
| Exact Mass | 203.131 Da |
| Monoisotopic Mass | 203.131 Da |
| Topological Polar Surface Area | 20.300 Ų |
| Heavy Atom Count | 15 |
| Formal Charge | 0 |
| Complexity | 201.000 |
| 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 |