Cinnamamide - CAS 621-79-4
Catalog: |
BB031452 |
Product Name: |
Cinnamamide |
CAS: |
621-79-4 |
Synonyms: |
3-Phenyl-2-propenamide; 2-Benzylideneacetamide; 3-Phenylpropenamide; 3-Phenylacrylamide; Cinnamic acid amide |
IUPAC Name: | 3-phenylprop-2-enamide |
Description: | Cinnamamide also called 3-Phenyl-2-propenamide, is natural phenylpropanoid isolated from the root of Kaempferia galangal L. 3-Phenyl-2-propenamide derivatives exhibits therapeutic potential in animal models of both central and peripheral nervous system disorders. |
Molecular Weight: | 147.17 |
Molecular Formula: | C9H9NO |
Canonical SMILES: | O=C(N)C=CC=1C=CC=CC1 |
InChI: | InChI=1S/C9H9NO/c10-9(11)7-6-8-4-2-1-3-5-8/h1-7H,(H2,10,11) |
InChI Key: | APEJMQOBVMLION-UHFFFAOYSA-N |
Boiling Point: | 350.3 °C at 760 mmHg |
Melting Point: | 149 °C |
Purity: | > 98 % |
Density: | 1.121 g/cm3 |
Appearance: | White crystal |
Storage: | Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances. |
MDL: | MFCD00008033 |
LogP: | 1.88540 |
GHS Hazard Statement: | H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral] |
Precautionary Statement: | P264, P270, P301+P312, P330, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
AU-2021104838-A4 | Mechanism of skin aging reversal by active ingredient WGX-50 of Zanthoxylum bungeanum Maxim | 20210802 |
CN-113480466-A | Indole substituted amide compound and preparation method and application thereof | 20210624 |
CN-113321825-A | Humic acid type bird-repelling pheromone core-shell structure gel and preparation method thereof | 20210528 |
CN-112939962-A | Benzofuran substituted amide compound and preparation method and application thereof | 20210204 |
CN-112694439-A | Phenyl acrylamide quinoline derivative and preparation method and application thereof | 20201231 |
PMID | Publication Date | Title | Journal |
29598909 | 20180515 | Dibenzofuran, dibenzothiophene and N-methyl carbazole tethered 2-aminothiazoles and their cinnamamides as potent inhibitors of Mycobacterium tuberculosis | Bioorganic & medicinal chemistry letters |
24937185 | 20140723 | Development of second generation EP2 antagonists with high selectivity | European journal of medicinal chemistry |
24530490 | 20140321 | Design, synthesis and antitubercular evaluation of novel series of N-[4-(piperazin-1-yl)phenyl]cinnamamide derivatives | European journal of medicinal chemistry |
22205092 | 20111228 | Neonaucline, a new indole alkaloid from the leaves of Ochreinauclea maingayii (Hook. f.) Ridsd. (Rubiaceae) | Molecules (Basel, Switzerland) |
21906854 | 20111101 | Synthesis and antimicrobial activity of amido linked pyrrolyl and pyrazolyl-oxazoles, thiazoles and imidazoles | European journal of medicinal chemistry |
Complexity: | 157 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 1 |
Exact Mass: | 147.068413911 |
Formal Charge: | 0 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 147.068413911 |
Rotatable Bond Count: | 2 |
Topological Polar Surface Area: | 43.1 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 1.4 |
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