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.