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1 References  














Idose






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From Wikipedia, the free encyclopedia
 


Idose[1]
Names
IUPAC name

Idose

Systematic IUPAC name

(3S,4R,5R,6R)-6-(Hydroxymethyl)oxane-2,3,4,5-tetrol

Identifiers

CAS Number

3D model (JSmol)

ChemSpider

PubChem CID

UNII
  • InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3+,4-,5+,6?/m1/s1 ☒N

    Key: WQZGKKKJIJFFOK-YIDFTEPTSA-N ☒N

  • InChI=1/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3+,4-,5+,6?/m1/s1

    Key: WQZGKKKJIJFFOK-YIDFTEPTBS

  • O[C@@H]1[C@@H](O)[C@H](OC(O)[C@H]1O)CO

Properties

Chemical formula

C6H12O6
Molar mass 180.156 g·mol−1

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

☒N verify (what is checkY☒N ?)

Infobox references

Idose is a hexose, a six carbon monosaccharide. It has an aldehyde group and is an aldose. It is not found in nature, but its uronic acid, iduronic acid, is important. It is a component of dermatan sulfate and heparan sulfate, which are glycosaminoglycans. The first and third hydroxyls point the opposite way from the second and fourth. It is made by aldol condensationofD- and L-glyceraldehyde. L-Idose is a C-5 epimerofD-glucose.

References

[edit]
  1. ^ Merck Index, 11th Edition, 4818
  • t
  • e

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Idose&oldid=1181944835"

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    This page was last edited on 26 October 2023, at 04:40 (UTC).

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