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3-O-METHYL-ALPHA-D-GLUCOPYRANOSE
  • Chemical Name: 3-O-METHYL-ALPHA-D-GLUCOPYRANOSE
  • CAS No.: 13224-94-7

Cost-effective customized wholesale 3-O-METHYL-ALPHA-D-GLUCOPYRANOSE 13224-94-7

  • Molecular Formula: C7H14O6
  • Molecular Weight: 194.185
  • Appearance/Colour: white fine crystalline powder 
  • Vapor Pressure: 0mmHg at 25°C 
  • Melting Point: 167-169 °C(lit.) 
  • Refractive Index: 1.548 
  • Boiling Point: 406.3 °C at 760 mmHg 
  • PKA: 12.05±0.70(Predicted) 
  • Flash Point: 199.5 °C 
  • PSA: 99.38000 
  • Density: 1.47g/cm3 
  • LogP: -2.56730 

3-O-METHYL-ALPHA-D-GLUCOPYRANOSE(Cas 13224-94-7) Usage

InChI:InChI=1/C7H14O6/c1-12-6-4(9)3(2-8)13-7(11)5(6)10/h3-11H,2H2,1H3/t3-,4-,5-,6+,7-/m1/s1

13224-94-7 Relevant articles

Systematic Hydrogen-Bond Manipulations To Establish Polysaccharide Structure–Property Correlations

Bordoni, Vittorio,Delbianco, Martina,Fair, Richard J.,Fittolani, Giulio,Grafmüller, Andrea,Seeberger, Peter H.,Singhal, Ankush,Tyrikos-Ergas, Theodore,Yu, Yang,Zhu, Yuntao

, p. 13127 - 13132 (2019)

A dense hydrogen-bond network is respons...

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De,K.K.,Timell,T.E.

, p. 72 - 77 (1967)

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A sulfated galactan with antioxidant capacity from the green variant of tetrasporic Gigartina skottsbergii (Gigartinales, Rhodophyta)

Barahona, Tamara,Encinas, María V.,Mansilla, Andrés,Matsuhiro, Betty,Zú?iga, Elisa A.

experimental part, p. 114 - 120 (2012/03/22)

The water soluble polysaccharide produce...

The Synthesis and Reactivity of Cyclic Thiocarbonates Derived from Some Carbohydrate 1,2-Diols

Patroni, Joseph J.,Stick, Robert V.,Tilbrook, D. Matthew G.,Skelton, Brian W.,White, Allan H.

, p. 2127 - 2141 (2007/10/02)

The attempted synthesis of several carbo...

Studies on synthesis of 3-O-alkyl-D-glucose and 3-O-alkyl-D-allose derivatives and their biological activities

Ikekawa,Irinoda,Saze,Katori,Matsuda,Ohkawa,Kosik

, p. 2894 - 2899 (2007/10/02)

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13224-94-7 Process route

(3aR,5R,6S,6aR)-5-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)-6-methoxy-2,2-dimethyltetrahydrofuro[2,3-d][1,3]-dioxol
97834-06-5

(3aR,5R,6S,6aR)-5-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)-6-methoxy-2,2-dimethyltetrahydrofuro[2,3-d][1,3]-dioxol

3-O-methyl-D-glucose
13224-94-7

3-O-methyl-D-glucose

3-O-methyl-β-D-glucopyranose
13224-95-8

3-O-methyl-β-D-glucopyranose

Conditions
Conditions Yield
With Amberlite IR-120 (H+ form); In water; at 80 ℃; for 16h; Overall yield = 100 percent; Overall yield = 39.6 mg;
1,2:5,6-di-O-isopropylidene-α-D-glucofuranose
582-52-5

1,2:5,6-di-O-isopropylidene-α-D-glucofuranose

3-O-methyl-D-glucose
13224-94-7

3-O-methyl-D-glucose

Conditions
Conditions Yield
(methylation);

13224-94-7 Upstream products

  • 582-52-5
    582-52-5

    1,2:5,6-di-O-isopropylidene-α-D-glucofuranose

  • 97834-06-5
    97834-06-5

    (3aR,5R,6S,6aR)-5-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)-6-methoxy-2,2-dimethyltetrahydrofuro[2,3-d][1,3]-dioxol

  • 54649-66-0
    54649-66-0

    1,2:5,6-di-O-isopropylidene-α-D-gulose

  • 29587-01-7
    29587-01-7

    5-[2,2-dimethyl-(4R)-1,3-dioxolan-4-yl]-2,2-dimethyl-(3aR,5R,6R,6aR)-perhydrofuro[2,3-d][1,3]dioxol-6-yl methyl ether

13224-94-7 Downstream products

  • 126874-18-8
    126874-18-8

    (S,S)-1,2:4,6-di-O-benzylidene-3-O-methyl-α-D-gulose

  • 126797-42-0
    126797-42-0

    (S)-4,6-O-benzylidene-3-O-methyl-D-gulose

  • 195703-49-2
    195703-49-2

    Benzoic acid (S)-((4S,4aS,8aR,9R,9aR,10aR)-9-methoxy-7,7-dimethyl-hexahydro-1,3,6,8,10-pentaoxa-anthracen-4-ylcarbamoyl)-((2R,5R,6R)-2-methoxy-5,6-dimethyl-4-methylene-tetrahydro-pyran-2-yl)-methyl ester

  • 195703-50-5
    195703-50-5

    Benzoic acid (S)-((4R,4aS,8aR,9R,9aR,10aR)-9-methoxy-7,7-dimethyl-hexahydro-1,3,6,8,10-pentaoxa-anthracen-4-ylcarbamoyl)-((2R,5R,6R)-2-methoxy-5,6-dimethyl-4-methylene-tetrahydro-pyran-2-yl)-methyl ester