≥98%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C Ships Wet ice 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.
N,N-Diethyl-2-cyanoacetoamide can be used:
· To prepare N,N-diethyl 2-cyano-2-fluoro-2-phenylthioacetoamide, which is further used in the synthesis of various cyanofluoroamides.
· In the synthesis of entacapone, a catechol-O-methyltransferase inhibitor by reacting with 3,4-dihydroxy-5-nitrobenzaldehyde.
· As a building block in the synthesis of fluorophores, applicable as endoplasmic reticulum probes.
| Pubchem Sid | 504762770 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504762770 |
| Canonical Smiles | CCN(CC)C(=O)CC#N |
| IUPAC Name | 2-cyano-N,N-diethylacetamide |
| InChIKey | RYSHIRFTLKZVIH-UHFFFAOYSA-N |
| INCHI | 1S/C7H12N2O/c1-3-9(4-2)7(10)5-6-8/h3-5H2,1-2H3 |
| Isomeric SMILES | CCN(CC)C(=O)CC#N |
| WGK Germany | 3 |
| Molecular Weight | 140.19 |
| Reaxy-Rn | 2204937 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2204937&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 acids and derivatives |
| Class | Carboxylic acids and derivatives |
| Subclass | Carboxylic acid derivatives |
| Intermediate Tree Nodes | Carboxylic acid amides |
| Direct Parent | Tertiary carboxylic acid amides |
| Alternative Parents | Nitriles Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Tertiary carboxylic acid amide - Nitrile - Carbonitrile - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as tertiary carboxylic acid amides. These are compounds containing an amide derivative of carboxylic acid, with the general structure RN(R1)C(R2)=O (R1-R2 any atom but H). |
| External Descriptors | monocarboxylic acid amide - aliphatic nitrile |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 F2224028 | Certificate of Analysis | Apr 02, 2026 | C153738 |
| F2224434 | Certificate of Analysis | Apr 02, 2026 | C153738 |
| F2224435 | Certificate of Analysis | Apr 02, 2026 | C153738 |
| L2117024 | Certificate of Analysis | Oct 11, 2025 | C153738 |
| J2109170 | Certificate of Analysis | Jul 10, 2025 | C153738 |
| J2109171 | Certificate of Analysis | Jul 10, 2025 | C153738 |
| J2109173 | Certificate of Analysis | Jul 10, 2025 | C153738 |
| J2109198 | Certificate of Analysis | Jul 10, 2025 | C153738 |
| Sensitivity | heat sensitive |
|---|---|
| Refractive Index | 1.47 |
| Flash Point(°F) | >230 °F |
| Flash Point(°C) | >110 °C |
| Boil Point(°C) | 114°C/4mmHg(lit.) |
| Molecular Weight | 140.180 g/mol |
| XLogP3 | 0.300 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 3 |
| Exact Mass | 140.095 Da |
| Monoisotopic Mass | 140.095 Da |
| Topological Polar Surface Area | 44.100 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 152.000 |
| 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 |
