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Record Information |
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| Version |
1.0 |
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| Update Date |
1/22/2018 11:54:54 AM |
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Metabolite ID | PAMDB120173 |
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Identification |
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| Name: |
propionamide |
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| Description: | A monocarboxylic acid amide obtained by the formal condensation of propionic acid with ammonia. |
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Structure |
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| Synonyms: | - n-propionic amide
- Propanimidic acid
- PROPIONAMIDE
- Propionic acid amide
- Propionic amide
- propionic amide
- Propionimidic acid
- Propylamide
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Chemical Formula: |
C3H7NO |
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| Average Molecular Weight: |
73.094 |
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| Monoisotopic Molecular
Weight: |
73.052765 |
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| InChI Key: |
QLNJFJADRCOGBJ-UHFFFAOYSA-N |
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| InChI: | InChI=1S/C3H7NO/c1-2-3(4)5/h2H2,1H3,(H2,4,5) |
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| CAS
number: |
Not Available |
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| IUPAC Name: | propanamide |
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Traditional IUPAC Name: |
Not Available |
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| SMILES: | CCC(N)=O |
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Chemical Taxonomy |
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Taxonomy Description | This compound belongs to the class of organic compounds known as primary carboxylic acid amides. These are compounds comprising primary carboxylic acid amide functional group, with the general structure RC(=O)NH2. |
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Kingdom |
Organic compounds |
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| Super Class | Organic acids and derivatives |
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Class |
Carboxylic acids and derivatives |
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| Sub Class | Carboxylic acid derivatives |
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Direct Parent |
Primary carboxylic acid amides |
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| Alternative Parents |
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| Substituents |
- Primary carboxylic acid amide
- Organic nitrogen compound
- Organic oxygen compound
- Organopnictogen compound
- Organic oxide
- Hydrocarbon derivative
- Organooxygen compound
- Organonitrogen compound
- Carbonyl group
- Aliphatic acyclic compound
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| Molecular Framework |
Aliphatic acyclic compounds |
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| External Descriptors |
- monocarboxylic acid amide (CHEBI:45422)
- a small molecule (PROPIONAMIDE)
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Physical Properties |
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| State: |
Not Available |
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| Charge: | 0 |
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Melting point: |
Not Available |
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| Experimental Properties: |
Not Available |
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| Predicted Properties |
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Biological Properties |
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| Cellular Locations: |
Not Available |
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| Reactions: | |
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Pathways: |
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Spectra |
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| Spectra: |
Not Available |
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References |
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| References: |
- 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, Pubmed: 24723348
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| Synthesis Reference: |
Not Available |
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| Material Safety Data Sheet (MSDS) |
Not Available |
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Links |
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| External Links: |
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