α,β-1-Methyl-D-ribofuranoside
- Product Name
- α,β-1-Methyl-D-ribofuranoside
- CAS No.
- 13039-63-9
- Chemical Name
- α,β-1-Methyl-D-ribofuranoside
- Synonyms
- (2R,3S,4R)-2-(Hydroxymethyl)-5-methoxytetrahydrofuran-3,4-diol;Methyl D-ribofuranoside(α and β mixture);AzacitidineImpurity46;α,β-1-Methyl-D-ribofuranoside;α,β-1-Methyl-D-ribofuranoside;(2R,3S,4R)-2-(Hydroxymethyl)-5-methoxytetrahydrofuran-3,4-diol(α and β mixture)
- CBNumber
- CB32603556
- Molecular Formula
- C6H12O5
- Formula Weight
- 164.16
- MOL File
- 13039-63-9.mol
α,β-1-Methyl-D-ribofuranoside Property
- storage temp.
- Sealed in dry,Room Temperature
- Stability:
- Hygroscopic
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
- Precautionary statements
-
P280Wear protective gloves/protective clothing/eye protection/face protection.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- 5558AA
- Product name
- (2R,3S,4R)-2-(Hydroxymethyl)-5-methoxytetrahydrofuran-3,4-diol
- Packaging
- 5g
- Price
- $492
- Updated
- 2021/12/16
- Product number
- CRB0005204
- Product name
- (2R,3S,4R)-2-(HYDROXYMETHYL)-5-METHOXYTETRAHYDROFURAN-3,4-DIOL
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $497.57
- Updated
- 2021/12/16
- Product number
- A134503
- Product name
- MethylD-ribofuranoside(αandβmixture)
- Purity
- 97%
- Packaging
- 250mg
- Price
- $113
- Updated
- 2021/12/16
- Product number
- CM196174
- Product name
- (2R,3S,4R)-2-(hydroxymethyl)-5-methoxytetrahydrofuran-3,4-diol
- Purity
- 95%
- Packaging
- 1g
- Price
- $122
- Updated
- 2021/12/16
- Product number
- SY111642
- Product name
- (2R,3S,4R)-2-(Hydroxymethyl)-5-methoxytetrahydrofuran-3,4-diol
- Purity
- ≥95%
- Packaging
- 5g
- Price
- $320
- Updated
- 2021/12/16
α,β-1-Methyl-D-ribofuranoside Chemical Properties,Usage,Production
Uses
Methyl D-Ribofuranoside is used in the preparation of antiviral nucleosides and derivatives thereof.
Synthesis
67-56-1
532-20-7
1824-96-0
General procedure for the synthesis of methyl α-D-xylofuranoside from methanol and 2-furancarboxylic acid (CAS:532-20-7): D-ribose (500 g, 3.33 mol) was dissolved in 1.5 L of anhydrous methanol containing 0.5% (v/v) hydrochloric acid, and the reaction system was placed in a round-bottomed flask fitted with a drying tube of calcium carbonate, and the reaction was stirred for 48 h at room temperature. Upon completion of the reaction, the pH of the reaction mixture was adjusted to 7 using Dowex (OH type) ion exchange resin to neutralize the acidity. Subsequently, the resin was removed by filtration, the filtrate was concentrated under reduced pressure to remove the solvent, and the resulting residue was dried under vacuum overnight to afford methyl α-D-xylofuranoside (550 g, 98% yield).
References
[1] European Journal of Organic Chemistry, 2006, # 14, p. 3152 - 3168
[2] Angewandte Chemie - International Edition, 2017, vol. 56, # 39, p. 11963 - 11965
[3] Angew. Chem., 2017, vol. 129, # 39, p. 12125 - 12127,3
[4] Tetrahedron, 1992, vol. 48, # 41, p. 9033 - 9072
[5] Patent: WO2005/27962, 2005, A1. Location in patent: Page/Page column 69-70
α,β-1-Methyl-D-ribofuranoside Preparation Products And Raw materials
Raw materials
Preparation Products
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