Methyl-α-D-Glucopyranoside

Basic information

  • Product Name:Methyl-α-D-Glucopyranoside
  • CasNo.:97-30-3
  • MF:C7H14O6
  • MW:194.185

Physical and Chemical Properties

  • Boiling Point:169-171 °C(lit.)
  • Packing:
  • Throughput:
Inquiry

Product Details

CasNo: 97-30-3

MF: C7H14O6

Appearance: White Powder

Factory supply Methyl-α-D-Glucopyranoside 97-30-3 with sufficient production capacity

  • Molecular Formula:C7H14O6
  • Molecular Weight:194.185
  • Appearance/Colour:White Powder 
  • Vapor Pressure:1.15E-07mmHg at 25°C 
  • Melting Point:169-171 °C(lit.) 
  • Refractive Index:157.5 ° (C=10, H2O) 
  • Boiling Point:389.1 °C at 760 mmHg 
  • PKA:pKa (25°): 13.71 
  • Flash Point:189.1 °C 
  • PSA:99.38000 
  • Density:1.47 g/cm3 
  • LogP:-2.56730 

alpha-D-Methylglucoside(Cas 97-30-3) Usage

Flammability and Explosibility

Notclassified

Purification Methods

Crystallise methyl -D-glucoside from MeOH or EtOH. Its solubility in H2O is 10%. [Ferrier et al. Carbohydr Research 27 55,59 1973, Beilstein 17/7 V 13.]

Definition

ChEBI: An alpha-D-glucopyranoside having a methyl substituent at the anomeric position.

InChI:InChI=1/C7H13O6/c1-12-6-5(10)4(9)3(2-8)13-7(6)11/h3-10H,2H2,1H3/q-1/t3-,4-,5+,6-,7+/m1/s1

97-30-3 Relevant articles

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Wolfrom,Gillam

, p. 3564 (1961)

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ESIMS and NMR studies on the selective deprotection of acetylated glucosides by dibutyltin oxide

Wang, Shao-Min,Zhu, Wei-Guo,Kang, Jian-Xun,Liu, Hong-Min,Chen, Jun-Miao,Li, Cui-Ping,Zhang, Kai

, p. 203 - 209 (2011)

The reaction process for the selective d...

Access to septanoside diacetals from methyl α-D-glucopyranoside

Contour, Marie-Odile,Fayet, Catherine,Gelas, Jacques

, p. 150 - 152 (1990)

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Direct Highly Regioselective Functionalization of Carbohydrates: A Three-Component Reaction Combining the Dissolving and Catalytic Efficiency of Ionic Liquids

Axelsson, Anton,Ta, Linda,Sundén, Henrik

, p. 3339 - 3343 (2016)

An unprecedented regioselective function...

A simple method for detritylation of carbohydrate derivatives

Randazzo, Giacomino,Capasso, Renato,Cicala, M. Rosaria,Evidente, Antonio

, p. 298 - 301 (1980)

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Biosynthesis of methyl glucoside and its antibacterial activity against Staphylococcus aureus and Escherichia coli

Kaulpiboon, Jarunee,Rudeekulthamrong, Prakarn

, (2019)

In this study, the methyl glucosides (MG...

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Karrer

, p. 1353,1366 (1943)

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Debenzylation of complex oligosaccharides using ferric chloride

Rodebaugh, Robert,Debenham, John S.,Fraser-Reid, Bert

, p. 5477 - 5478 (1996)

Anhydrous FeCl3 in CH2Cl2 at room temper...

Loss of C-5 hydrogen during conversion of d-glucuronic acid into methyl α-d-glucopyranoside

Prihar, Harry S.,Meganathan, Rangaswamy,Sidney Feingold, David

, p. 271 - 274 (1978)

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Triethylamine-methanol mediated selective removal of oxophenylacetyl ester in saccharides

Rasool, Javeed Ur,Kumar, Atul,Ali, Asif,Ahmed, Qazi Naveed

, p. 338 - 347 (2021/01/29)

A highly selective, mild, and efficient ...

SELECTIVE VALORIZATION OF BIOMASS SUGARS

-

Page/Page column 47-51, (2021/06/26)

Disclosed are methods of forming an epim...

Carbon glycoside glycosylated tetravalent platinum compound as well as synthesis method and application thereof

-

Paragraph 0064-0067, (2021/07/08)

The invention provides a carbon glycosid...

Calixanthomycin A: Asymmetric Total Synthesis and Structural Determination

Chen, Kuanwei,Xie, Tao,Shen, Yanfang,He, Haibing,Zhao, Xiaoli,Gao, Shuanhu

supporting information, p. 1769 - 1774 (2021/03/08)

We report the first asymmetric total syn...

97-30-3 Process route

methyl α-D-glucopyranoside 6-(S-benzyl xanthate)
17460-27-4

methyl α-D-glucopyranoside 6-(S-benzyl xanthate)

phenylmethanethiol
100-53-8

phenylmethanethiol

methyl-alpha-D-glucopyranoside
97-30-3

methyl-alpha-D-glucopyranoside

Conditions
Conditions Yield
With water; In methanol; at 35 ℃; Kinetics;
medalose

medalose

N-acetyl-D-glucosamine
14131-68-1

N-acetyl-D-glucosamine

β-D-glucose
492-61-5

β-D-glucose

alpha-D-glucopyranose
492-62-6

alpha-D-glucopyranose

β-D-galactopyranoside
7296-64-2

β-D-galactopyranoside

methyl beta-D-glucopyranoside
709-50-2

methyl beta-D-glucopyranoside

methyl-alpha-D-glucopyranoside
97-30-3

methyl-alpha-D-glucopyranoside

Conditions
Conditions Yield
With sulfuric acid; In 1,4-dioxane; at 50 ℃; for 22h;

97-30-3 Upstream products

  • 67-56-1
    67-56-1

    methanol

  • 50-99-7
    50-99-7

    D-glucose

  • 6936-67-0
    6936-67-0

    D-Glucose-dibenzyldithioacetal

  • 186581-53-3
    186581-53-3

    diazomethane

97-30-3 Downstream products

  • 18486-51-6
    18486-51-6

    1-O-methyl-α-D-glucopyranuronic acid methyl ester

  • 20550-17-8
    20550-17-8

    Methyl-<4,6-dichlor-bis-O-(toluol-4-sulfonyl)-4,6-didesoxy-α-D-galactopyranosid>

  • 19186-54-0
    19186-54-0

    methyl-[4-chloro-tris-O-(toluene-4-sulfonyl)-4-deoxy-α-D-galactopyranoside]

  • 49617-11-0
    49617-11-0

    methyl-[tetrakis-O-(toluene-4-sulfonyl)-α-D-glucopyranoside]