Chemistry:Benzamide
From HandWiki
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| Names | |
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| Preferred IUPAC name
Benzamide[1] | |
| Systematic IUPAC name
Benzenecarboxamide | |
| Other names
Benzoic acid amide
Phenyl carboxamide Benzoylamide | |
| Identifiers | |
3D model (JSmol)
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| 3DMet | |
| 385876 | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| EC Number |
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| KEGG | |
PubChem CID
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| RTECS number |
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| UNII | |
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| Properties | |
| C7H7NO | |
| Molar mass | 121.139 g·mol−1 |
| Appearance | Off-white solid |
| Density | 1.341 g/cm3 |
| Melting point | 127 to 130 °C (261 to 266 °F; 400 to 403 K) |
| Boiling point | 288 °C (550 °F; 561 K) |
| 13.5 g/L (at 25°C)[2] | |
| Acidity (pKa) | |
| -72.3·10−6 cm3/mol | |
| Pharmacology | |
| 1=ATC code }} | N05AL (WHO) |
| Hazards | |
| GHS pictograms |  
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| GHS Signal word | Warning |
| H302, H341 | |
| P201, P202, P264, P270, P281, P301+312, P308+313, P330, P405, P501 | |
| NFPA 704 (fire diamond) | |
| Flash point | 180 °C (356 °F; 453 K) |
| > 500 °C (932 °F; 773 K) | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is   ?)
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| Infobox references | |
Tracking categories (test):
Benzamide is an organic compound with the chemical formula of C7H7NO. It is the simplest amide derivative of benzoic acid. In powdered form, it appears as a white solid, while in crystalline form, it appears as colourless crystals.[5] It is slightly soluble in water,[2] and soluble in many organic solvents.[6] It is a natural alkaloid found in the herbs of Berberis pruinosa.[6]
Chemical derivatives
A number of substituted benzamides are commercial drugs, including:
See also
References
- ↑ Favre, Henri A.; Powell, Warren H. (2014). Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. p. 841. doi:10.1039/9781849733069-FP001. ISBN 9780854041824. OCLC 1077224056. https://books.google.com/books?id=4USgAgAAQBAJ. Retrieved 2022-10-11.
- ↑ 2.0 2.1 "Benzamide | 55-21-0 supplier and manufacturer". https://www.buyersguidechem.com/chemical_supplier/benzamide#:~:text=soluble,25%C2%B0%20C.
- ↑ Haynes, William M., ed (2016). CRC Handbook of Chemistry and Physics (97th ed.). CRC Press. p. 5–89 [sic]. ISBN 9781498754286. OCLC 1012162798. https://books.google.com/books?id=VVezDAAAQBAJ&dq=benzamide&pg=PA5-89. Retrieved 2022-10-11. page cited is 5-89, not 5 to 89
- ↑ Bordwell, Frederick G.; Ji, Guo Zhen (October 1991). "Effects of structural changes on acidities and homolytic bond dissociation energies of the hydrogen-nitrogen bonds in amidines, carboxamides, and thiocarboxamides". Journal of the American Chemical Society 113 (22): 8398–8401. doi:10.1021/ja00022a029. https://pubs.acs.org/doi/abs/10.1021/ja00022a029. Retrieved 2022-10-11.
- ↑ CID 2331 from PubChem
- ↑ 6.0 6.1 "benzamide, CAS number 55-21-0". https://www.thegoodscentscompany.com/data/rw1221711.html#:~:text=it%20is,organic%20solvents..
- ↑ Kent, James A.; Singh, K. N.; Merchant, Kavita (2012). "The Agrochemical Industry, Annex 17.1". in Kent, James A.. Handbook of Industrial Chemistry and Biotechnology. New York: Springer Verlag. pp. 643–698. doi:10.1007/978-1-4614-4259-2_17. ISBN 9781461442592. OCLC 1097100876. https://books.google.com/books?id=7VxDAAAAQBAJ&pg=PA693. Retrieved 2022-10-11.
External links
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