Edge Rewrite
// HTMLRewriter · presentation

This page was redesigned at the edge.

Cloudflare fetched the original article and streamed it through HTMLRewriter to apply an entirely new visual system without rebuilding the source page.

// request.cf · coarse context

A page that knows where it met you.

Only coarse request metadata is shown. This demo does not display or persist visitor IP addresses.

Country
US
Cloudflare location
CMH
Connection
HTTP/2
Language
Not provided

Ray ID: a235a1018b671528

Jump to content

// Workers AI · dad joke modeWhat did fucitol say to its friend? "You're a real sugar to me.

From Wikipedia, the free encyclopedia
Fucitol
Names
IUPAC name
1-Deoxy-L-galactitol
Systematic IUPAC name
(2R,3S,4R,5S)-Hexane-1,2,3,4,5-pentol
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
UNII
  • InChI=1S/C6H14O5/c1-3(8)5(10)6(11)4(9)2-7/h3-11H,2H2,1H3/t3-,4+,5-,6-/m0/s1 X markN
    Key: SKCKOFZKJLZSFA-FSIIMWSLSA-N X markN
  • C[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)CO
Properties
C6H14O5
Molar mass 166.17 g/mol
Melting point 153 to 154 °C (307 to 309 °F; 426 to 427 K)[1]
Supplementary data page
Fucitol (data page)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
X markN verify (what is checkYX markN ?)

Fucitol, also known as L-fucitol, 1-deoxy-L-galactitol, and (2R,3S,4R,5S)-hexane-1,2,3,4,5-pentol, is a sugar alcohol derived from fucoidan which is found in the North Atlantic seaweed Fucus vesiculosus[2] or by the reduction of fucose.[1]

See also

[edit]

References

[edit]
  1. 1 2 Votocek, Emil; Potmesil, R. Prag (1914). "Fucitol". Berichte der Deutschen Chemischen Gesellschaft. 46: 3653–3655. doi:10.1002/cber.191304603151.
  2. O'Neill, A. N. (1954). "Degradative studies on fucoidin". Journal of the American Chemical Society. 76 (20): 5074–5076. Bibcode:1954JAChS..76.5074O. doi:10.1021/ja01649a018.
[edit]
  • Wikimedia Commons logo Media related to Fucitol at Wikimedia Commons