Ammonium cinnamate

Last updated
Ammonium cinnamate
Ammonium cinnamate.svg
Names
IUPAC name
azanium;3-phenylprop-2-enoate
Identifiers
3D model (JSmol)
ChemSpider
PubChem CID
  • InChI=1S/C9H8O2.H3N/c10-9(11)7-6-8-4-2-1-3-5-8;/h1-7H,(H,10,11);1H3/b7-6+;
    Key: PBLWYVAEJYQTLU-UHDJGPCESA-N
  • C1=CC=C(C=C1)C=CC(=O)[O-].[NH4+]
Properties
C9H11NO2
Molar mass 165.192 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Ammonium cinnamate is an organic chemical compound with the chemical formula C9H11NO2. This is an organic ammonium salt of cinnamic acid. [1] [2] [3]

Contents

Synthesis

The compound can be obtained via reaction of ammonia with aqueous solution of cinnamic acid. [4]

Uses

The compound is used in chemical synthesis and pharmaceutical applications. [5] [6] [7]

References

  1. ↑ "Ammonium cinammate". NIST . Retrieved 29 March 2025.
  2. ↑ "Chemical Properties of Ammonium cinnamate (CAS 25459-05-6)". chemeo.com. Retrieved 29 March 2025.
  3. ↑ Nord, F. F. (10 September 2009). Advances in Enzymology and Related Areas of Molecular Biology. John Wiley & Sons. p. 94. ISBN   978-0-470-12329-4 . Retrieved 29 March 2025.
  4. ↑ Streatfeild, Frederick William (1891). Practical Work in Organic Chemistry. E. & F.N. Spon. p. 145. Retrieved 29 March 2025.
  5. ↑ The Journal of Analytical Chemistry of the USSR. Consultants Bureau. July 1969. p. 985. Retrieved 30 March 2025.
  6. ↑ Nuclear Science Abstracts. Oak Ridge Directed Operations, Technical Information Division. 1974. p. 263. Retrieved 30 March 2025.
  7. ↑ Goswami, Animesh; Stewart, Jon D. (6 September 2015). Organic Synthesis Using Biocatalysis. Academic Press. p. 390. ISBN   978-0-12-411542-2 . Retrieved 30 March 2025.
This page is based on this Wikipedia article
Text is available under the CC BY-SA 4.0 license; additional terms may apply.
Images, videos and audio are available under their respective licenses.