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ChemicalBook--->CAS DataBase List--->868156-46-1

868156-46-1

868156-46-1 Structure

868156-46-1 Structure
IdentificationBack Directory
[Name]

(S)-Pro-xylane (Synonyms: (S)-Hydroxypropyl tetrahydropyrantriol)
[CAS]

868156-46-1
[Synonyms]

(S)-Pro-xylane
L-glycero-L-gluco-Octitol, 1,5-anhydro-6,8-dideoxy-
(S)-Pro-xylane (Synonyms: (S)-Hydroxypropyl tetrahydropyrantriol)
[EINECS(EC#)]

456-880-5
[Molecular Formula]

C8H16O5
[MOL File]

868156-46-1.mol
[Molecular Weight]

192.21
Chemical PropertiesBack Directory
[Boiling point ]

376.0±42.0 °C(Predicted)
[density ]

1.368±0.06 g/cm3(Predicted)
[storage temp. ]

4°C, away from moisture and light
[solubility ]

DMSO: 250 mg/mL (1300.66 mM)
[form ]

Solid
[pka]

13.55±0.70(Predicted)
[color ]

White to off-white
[InChI]

InChI=1/C8H16O5/c1-4(9)2-6-8(12)7(11)5(10)3-13-6/h4-12H,2-3H2,1H3/t4-,5+,6-,7-,8-/s3
[InChIKey]

KOGFZZYPPGQZFZ-FHYXRTTRNA-N
[SMILES]

C([C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O)[C@@H](O)C |&1:1,4,6,8,10,r|
Hazard InformationBack Directory
[Description]

(S)-Pro-xylane is the S-enantiomer of Pro-xylane. Pro-xylane, a biologically active C-glycoside in aqueous media, acts as an activator of glycosaminoglycans (GAGs) biosynthesis.
[Synthesis]

In the autoclave, add 461g of intermediate 2,5 liters of isopropanol sequentially, seal the autoclave, replace the nitrogen 3 times, hydrogen displace 1 time, and then dissolve the catalyst [RuCl(cymene)(S-BINAP)] Cl (300mg) in 300mL of isopropanol solution underH2atmosphere, carefully add it to the autoclave, continue to fill hydrogen to 50kgf/cm2, and then heat up to about 60 °C, After stirring the reaction for 6h, stop the reaction, remove the material, and cool down the crystals to obtain βS-type Boseine products.The final product (S)-Pro-xylane can be obtained.
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