44627
D-Fructopyranose 2-phosphate potassium salt
≥98.0% (TLC)
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About This Item
Empirical Formula (Hill Notation):
C6H13O9P · xK+
CAS Number:
Molecular Weight:
260.14 (free acid basis)
UNSPSC Code:
12352201
PubChem Substance ID:
NACRES:
NA.25
assay
≥98.0% (TLC)
storage temp.
−20°C
SMILES string
O[C@H]1[C@H](O)[C@H](O)CO[C@]1(OP(O)(O)=O)CO
InChI
1S/C6H13O9P/c7-2-6(15-16(11,12)13)5(10)4(9)3(8)1-14-6/h3-5,7-10H,1-2H2,(H2,11,12,13)/t3-,4?,5-,6+/m1/s1
InChI key
FKTOSTOKRBVXKU-CNKSGKBASA-N
Biochem/physiol Actions
Metabolite involved in the fructose and mannose system.
Storage Class
13 - Non Combustible Solids
wgk_germany
WGK 3
flash_point_c
Not applicable
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Preparation of glycosyl phosphates. Betad-fructopyranose 2-phosphate.
D L MacDonald
The Journal of organic chemistry, 31(2), 513-516 (1966-02-01)
C Degani et al.
Journal of molecular evolution, 6(1), 51-60 (1975-10-03)
Cyanogen-induced phosphorylation of D-fructose at pH 8.8 led to the formation of a phosphorylated sugar identified as alpha-D-furcto-pyranose 2-phosphate on the basis of its chromatographic and electrophoretic properties, its lability to hydrolysis by alkaline phosphatase, the rate of its acid-catalysed
Hydrolysis and Isomerization of Sugar Phosphates and Carbohydrate Phosphodiesters.
Mikkola, S.
Current Organic Chemistry, 17, 1525-1544 (2013)
Properties of D-fructose 1,2-cyclic phosphates and fructose 2-phosphates.
Taniguchi, H. and Nakamura, M.
Agricultural and Biological Chemistry, 36, 2373-2380 (1972)
SYNTHESIS OF D-FRUCTOPYRANOSE 2-PHOSPHATE AND D-FRUCTOFURANOSE 2-PHOSPHATE.
H G PONTIS et al.
The Biochemical journal, 89, 452-459 (1963-12-01)
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