Chebulic acid

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Chebulic acid
200px
Chebulic acid, according to Lee, 2010.[1]
Chebulic acid, according to Klika, 2004.
Chebulic acid, according to Klika, 2004.[2]
Names
IUPAC name
(2R)-2-[(3S)-3-carboxy-5,6,7-trihydroxy-1-oxo-3,4-ihydroisochromen-4-yl]butanedioic acid
Other names
Chebuloyl
Identifiers
23725-05-5 YesY
ChemSpider 27470963 N
Jmol 3D model Interactive image
PubChem 25255065
  • InChI=1S/C14H12O11/c15-5-1-4-7(10(19)9(5)18)8(3(12(20)21)2-6(16)17)11(13(22)23)25-14(4)24/h1,3,8,11,15,18-19H,2H2,(H,16,17)(H,20,21)(H,22,23)/t3-,8-,11-/m0/s1 N
    Key: COZMWVAACFYLBI-XJEVXTIOSA-N N
  • InChI=1/C14H12O11/c15-5-1-4-7(10(19)9(5)18)8(3(12(20)21)2-6(16)17)11(13(22)23)25-14(4)24/h1,3,8,11,15,18-19H,2H2,(H,16,17)(H,20,21)(H,22,23)/t3-,8-,11-/m0/s1
    Key: COZMWVAACFYLBI-XJEVXTIOBW
  • c1c2c(c(c(c1O)O)O)[C@@H]([C@H](OC2=O)C(=O)O)[C@H](CC(=O)O)C(=O)O
Properties
C14H12O11
Molar mass 356.23 g/mol
Appearance Brown powder
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Chebulic acid is a phenolic compound isolated from the ripe fruits of Terminalia chebula.[3]

This compound possesses an isomer, neochebulic acid.

Chebulic acid is a component of transformed ellagitannins such as chebulagic acid or chebulinic acid.

References

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