CHEBI:45422 - propionamide

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name propionamide
ChEBI ID CHEBI:45422
Definition A monocarboxylic acid amide obtained by the formal condensation of propionic acid with ammonia.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information ChemicalBook:CB7854392, eMolecules:481804, ZINC000001670847
Download Molfile XML SDF
more structures >>
Wikipedia License
Propanamide has the chemical formula CH3CH2C=O(NH2). It is the amide of propanoic acid. This organic compound is a mono-substituted amide. Organic compounds of the amide group can react in many different organic processes to form other useful compounds for synthesis.
Read full article at Wikipedia
Formula C3H7NO
Net Charge 0
Average Mass 73.09382
Monoisotopic Mass 73.05276
InChI InChI=1S/C3H7NO/c1-2-3(4)5/h2H2,1H3,(H2,4,5)
InChIKey QLNJFJADRCOGBJ-UHFFFAOYSA-N
SMILES CCC(N)=O
ChEBI Ontology
Outgoing propionamide (CHEBI:45422) has functional parent propionic acid (CHEBI:30768)
propionamide (CHEBI:45422) is a monocarboxylic acid amide (CHEBI:29347)
propionamide (CHEBI:45422) is a primary fatty amide (CHEBI:143129)
Incoming (2S)-2-[(3S)-3-{[(6-chloronaphthalen-2-yl)sulfonyl]amino}-2-oxopyrrolidin-1-yl]-N-(1-methylethyl)-N-{2-[(methylsulfonyl)amino]ethyl}propanamide (CHEBI:47440) has functional parent propionamide (CHEBI:45422)
N-[3-hydroxy-2-(7-methoxy-1-naphthyl)propyl]propionamide (CHEBI:48445) has functional parent propionamide (CHEBI:45422)
N-{4-[1-(phenylcarbonyl)piperidin-4-yl]butyl}-3-pyridin-3-ylpropanamide (CHEBI:41973) has functional parent propionamide (CHEBI:45422)
tasimelteon (CHEBI:79042) has functional parent propionamide (CHEBI:45422)
IUPAC Name
propanamide
Synonyms Sources
n-propionic amide ChEBI
propanamide UniProt
Propanimidic acid ChemIDplus
PROPIONAMIDE PDBeChem
Propionic acid amide ChemIDplus
Propionic amide ChemIDplus
propionic amide ChEBI
Propionimidic acid ChemIDplus
Propylamide ChemIDplus
Manual Xrefs Databases
Propionamide Wikipedia
PROPIONAMIDE MetaCyc
ROP PDBeChem
View more database links
Registry Numbers Types Sources
79-05-0 CAS Registry Number NIST Chemistry WebBook
79-05-0 CAS Registry Number ChemIDplus
969258 Reaxys Registry Number Reaxys
Citation
Sogani M, Bakre PP, Mathur N, Sharma P, Bhatnagar P (2014)
Acetamide hydrolyzing activity of Bacillus megaterium F-8 with bioremediation potential: optimization of production and reaction conditions.
Environmental science and pollution research international 21, 8822-8830 [PubMed:24723348]
[show Abstract]
Last Modified
29 November 2018