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m-Coumaric acid

From Wikipedia, the free encyclopedia
m-Coumaric acid
Skeletal formula of m-coumaric acid
Skeletal formula ofm-coumaric acid
Names
Preferred IUPAC name
(2E)-3-(3-Hydroxyphenyl)prop-2-enoic acid
Other names
meta-Coumaric acid
3-Hydroxycinnamic acid
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard100.008.742Edit this at Wikidata
EC Number
  • 209-615-0
KEGG
UNII
  • InChI=1S/C9H8O3/c10-8-3-1-2-7(6-8)4-5-9(11)12/h1-6,10H,(H,11,12)/b5-4+
    Key: KKSDGJDHHZEWEP-SNAWJCMRSA-N
  • InChI=1/C9H8O3/c10-8-3-1-2-7(6-8)4-5-9(11)12/h1-6,10H,(H,11,12)/b5-4+
    Key: KKSDGJDHHZEWEP-SNAWJCMRBO
  • C1=CC(=CC(=C1)O)/C=C/C(=O)O
Properties
C9H8O3
Molar mass164.16 g/mol
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

m-Coumaric acid is ahydroxycinnamic acid, an organic compound that is ahydroxy derivative ofcinnamic acid.[1] There are threeisomers ofcoumaric acido-coumaric acid,m-coumaric acid, andp-coumaric acid – that differ by the position of the hydroxy substitution of the phenyl group.

m-Coumaric acid can be found invinegar.

References

[edit]
  1. ^m-Coumaric acid at www.phenol-explorer.eu
Aglycones
Precursor
Monohydroxycinnamic acids
(Coumaric acids)
Dihydroxycinnamic acids
Trihydroxycinnamic acids
O-methylated forms
others
Esters
glycoside-likes
Esters of
caffeic acid
with cyclitols
esters of
quinic acid
esters of
shikimic acid
Glycosides
Tartaric acid esters
Other esters
with caffeic acid
Caffeoyl phenylethanoid
glycoside (CPG)
Oligomeric forms
Dimers
Trimers
Tetramers
Conjugates with
coenzyme A (CoA)


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