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Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Application
3-Dimethylaminoacrolein was used in synthesis of: benzochlorins, benzoisobacteriochlorins and benzobacteriochlorins styryl-substituted Z / E -chlorin derivatives with chlorophyll-a skeleton Y shaped cyanines having dimethylamino end groups
| Sonrisas canónicas | CN(C)C=CC=O |
|---|---|
| IUPAC Name | (E)-3-(dimethylamino)prop-2-enal |
| InChIKey | RRLMPLDPCKRASL-ONEGZZNKSA-N |
| INCHI | 1S/C5H9NO/c1-6(2)4-3-5-7/h3-5H,1-2H3/b4-3+ |
| Isómeros SMILES | CN(C)/C=C/C=O |
| WGK Alemania | 3 |
| Peso molecular | 99.13 |
| Beilstein | 969389 |
| Reaxy-Rn | 969389 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=969389&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 | Alpha,beta-unsaturated carbonyl compounds - Alpha,beta-unsaturated aldehydes |
| Direct Parent | Enals |
| Alternative Parents | Vinylogous amides Trialkylamines Enamines Allylamines Organopnictogen compounds Organic oxides Hydrocarbon derivatives Aldehydes |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Vinylogous amide - Enal - Tertiary aliphatic amine - Tertiary amine - Allylamine - Enamine - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Amine - Aldehyde - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as enals. These are an alpha,beta-unsaturated aldehyde of general formula RC=C-CH=O in which the aldehydic C=O function is conjugated to a C=C triple bond at the alpha,beta position. |
| 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 |
|---|---|---|---|
| Certificate of Analysis | Jul 04, 2025 | D434586 |
| Índice de refracción | 1.584 |
|---|---|
| Punto de ebullición (°C) | 91 °C/1 mmHg; |
| Peso molecular | 99.130 g/mol |
| XLogP3 | 0.100 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 2 |
| Exact Mass | 99.0684 Da |
| Monoisotopic Mass | 99.0684 Da |
| Topological Polar Surface Area | 20.300 Ų |
| Heavy Atom Count | 7 |
| Formal Charge | 0 |
| Complexity | 76.100 |
| 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 |