Acetamide - CAS 60-35-5
Catalog: |
BB030663 |
Product Name: |
Acetamide |
CAS: |
60-35-5 |
Synonyms: |
Ethanamide; Acetic Acid Amide; Methanecarboxamide; Acetimidic Acid; Amide C2 |
IUPAC Name: | acetamide |
Description: | Acetamide is the simplest amide derived from acetic acid. It finds some use as a plasticizer and as an industrial solvent. Acetamide (2.88 g/kg/d) can reduce central nervous lesions, but the efficacy is not improved after increasing the dose. |
Molecular Weight: | 59.07 |
Molecular Formula: | C2H5NO |
Canonical SMILES: | CC(=O)N |
InChI: | InChI=1S/C2H5NO/c1-2(3)4/h1H3,(H2,3,4) |
InChI Key: | DLFVBJFMPXGRIB-UHFFFAOYSA-N |
Boiling Point: | 221 °C |
Melting Point: | 78-81 °C |
Purity: | > 98 % |
Density: | 1.159 g/cm3 |
Solubility: | Soluble in Water |
Appearance: | White crystalline solid |
Storage: | Store at 2-8 °C |
Decomposition: | Hazardous decomposition products formed under fire conditions - carbon oxides, Nitrogen oxides (nox) |
MDL: | MFCD00008023 |
LogP: | -1.26 |
Quality Standard: | Enterprise Standard |
Refractive Index: | 1.4274 at 78 °C/D |
Stability: | Stable under recommended storage conditions |
Vapor Pressure: | 1 mmHg at 149 °F |
GHS Hazard Statement: | H351: Suspected of causing cancer [Warning Carcinogenicity] |
Precautionary Statement: | P201, P202, P281, P308+P313, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-108845126-A | A kind of chromatography and enzyme chemical method joint-detection gynecology colpitis kit | 20180627 |
CN-108845126-B | A kind of chromatography and enzyme chemical method joint-detection gynecology colpitis kit | 20180627 |
CN-108484467-A | A kind of preparation method of Oseltamivir acetylethyleneimine intermediate | 20180409 |
AU-2018349244-A1 | N-acetylneuraminic acid compositions and methods of use | 20171011 |
WO-2019073298-A1 | NEURAMINIC ACID COMPOSITIONS AND METHODS OF USE | 20171011 |
PMID | Publication Date | Title | Journal |
31881176 | 20200201 | A toxicogenomic approach for the risk assessment of the food contaminant acetamide | Toxicology and applied pharmacology |
31735575 | 20200101 | Fragment hopping-based discovery of novel sulfinylacetamide-diarylpyrimidines (DAPYs) as HIV-1 nonnucleoside reverse transcriptase inhibitors | European journal of medicinal chemistry |
30606670 | 20190201 | Design, synthesis and biological evaluation of novel acetamide-substituted doravirine and its prodrugs as potent HIV-1 NNRTIs | Bioorganic & medicinal chemistry |
28554091 | 20170908 | Design and synthesis of potent HIV-1 protease inhibitors with (S)-tetrahydrofuran-tertiary amine-acetamide as P2-ligand: Structure-activity studies and biological evaluation | European journal of medicinal chemistry |
28108177 | 20170301 | Discriminating between adaptive and carcinogenic liver hypertrophy in rat studies using logistic ridge regression analysis of toxicogenomic data: The mode of action and predictive models | Toxicology and applied pharmacology |
Complexity: | 33 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 59.037113783 |
Formal Charge: | 0 |
Heavy Atom Count: | 4 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 59.037113783 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 43.1 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | -0.9 |
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