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ChemicalBook >  Product Catalog >  Biochemical Engineering >  Saccharides >  Monosaccharide >  PHENYL 2,3,4,6-TETRA-O-ACETYL-1-THIO-BETA-D-GLUCOPYRANOSIDE

PHENYL 2,3,4,6-TETRA-O-ACETYL-1-THIO-BETA-D-GLUCOPYRANOSIDE

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PHENYL 2,3,4,6-TETRA-O-ACETYL-1-THIO-BETA-D-GLUCOPYRANOSIDE Basic information

Product Name:
PHENYL 2,3,4,6-TETRA-O-ACETYL-1-THIO-BETA-D-GLUCOPYRANOSIDE
Synonyms:
  • PHENYL 2,3,4,6-TETRA-O-ACETYL-1-THIO-BETA-D-GLUCOPYRANOSIDE
  • .beta.-D-Glucopyranoside, phenyl 1-thio-, tetraacetate
  • 1-phenyl-1-thio-β-d-glucopyranoside tetraacetate
  • Phenyl2,3,4,6-tetra-O-acetyl-b-D-thioglucopyranoside
  • PHENYL-2,3,4,6-TETRA-O-ACETYL-1-THIO-SS-D-GLUCOPYRANOSIDE
  • PHENYL 2,3,4,6-TETRA-O-ACETYL-1-THIO-BET
  • Phenyl-2,3,4,6-tetra-O-acetyl-1-thio-β-D-glucopyranosid
  • Phenyl 2,3,4,6-O-Tetraacetyl-1-thio-β-D-glucopyranoside
CAS:
23661-28-1
MF:
C20H24O9S
MW:
440.46
EINECS:
205-516-1
Product Categories:
  • Carbohydrates
  • Thioglycosides
  • Carbohydrate Synthesis
  • Monosaccharides
  • Specialty Synthesis
  • Biochemistry
  • Glucose
  • Glycosyl Donors
  • Sugars
Mol File:
23661-28-1.mol
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PHENYL 2,3,4,6-TETRA-O-ACETYL-1-THIO-BETA-D-GLUCOPYRANOSIDE Chemical Properties

Melting point:
116-119 °C(lit.)
Boiling point:
514.6±50.0 °C(Predicted)
Density 
1.31±0.1 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
solubility 
slightly sol. in Chloroform
form 
Powder
color 
White to Off-white
optical activity
[α]20/D 14°, c = 2 in chloroform
InChIKey
JCKOUAWEMPKIAT-WTJXOVOXSA-N
CAS DataBase Reference
23661-28-1
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Safety Information

Safety Statements 
24/25
WGK Germany 
3
HS Code 
29329990

MSDS

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PHENYL 2,3,4,6-TETRA-O-ACETYL-1-THIO-BETA-D-GLUCOPYRANOSIDE Usage And Synthesis

Chemical Properties

White to off-white powder

Uses

Phenyl 2,3,4,6-tetra-O-acetyl-β-D-thioglucopyranoside, 98% (PTATG, 98%) can be used in glycobiology research.

Synthesis

2936-70-1

108-24-7

13992-16-0

General procedure: 1,4-Diazabicyclo[2.2.2]octane (DABCO, 1.0 mole equivalent) was added to a suspension of (2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(phenylthio)tetrahydro-2H-pyran-3,4,5-triol (10.0 g, 51.5 mmol) in acetic anhydride (1.2 mole equivalents/hydroxy group) The mixture was stirred at room temperature. The progress of the reaction was monitored by thin layer chromatography (TLC) and the eluent was ethyl acetate:hexane (2:3). Upon completion of the reaction, the mixture was poured into crushed ice and stirred for a few minutes to induce precipitation of (2R,3R,4S,5R,6R)-2-(acetyloxymethyl)-6-(phenylthio)tetrahydro-2H-pyran-3,4,5-triyltriacetate, while the DABCO was dissolved in water (as confirmed by TLC and iodine vapor color development). The product was separated by diafiltration and subsequently washed with ice water and dried. The resulting product was pure enough to be used directly in the subsequent reaction in a yield of 18.3 g in 98% yield. Analytically pure samples can be obtained by recrystallization from 95% ethanol. It should be noted that the temperature of the reaction mixture increases during the addition of DABCO and stirring. In experiments on the scale of 10-20 g, this phenomenon favors a significant increase in the reaction rate. However, for larger scale reactions (50-100g and above), it is recommended to add DABCO in batches to avoid overheating the reaction mixture.

References

[1] Tetrahedron Letters, 2011, vol. 52, # 44, p. 5841 - 5846
[2] Carbohydrate Research, 2013, vol. 365, p. 14 - 19
[3] RSC Advances, 2015, vol. 5, # 15, p. 11687 - 11696
[4] Journal of the American Chemical Society, 1929, vol. 51, p. 3619,3623

PHENYL 2,3,4,6-TETRA-O-ACETYL-1-THIO-BETA-D-GLUCOPYRANOSIDESupplier

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