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Ethyl 1,3,4,6-tetra-O-acetylhex-2-ulofuranoside is a complex organic compound with the molecular formula C16H20O10. It is a derivative of a hexose sugar, specifically a furanose, which is a type of sugar molecule that forms a five-membered ring. The compound is characterized by the presence of four acetyl groups (-COCH3) attached to the hydroxyl groups (-OH) at the 1, 3, 4, and 6 positions of the hexose ring. The "2-ulofuranoside" part of the name indicates that there is a ketone group (C=O) at the 2 position, which is a key feature of this specific sugar derivative. ethyl 1,3,4,6-tetra-O-acetylhex-2-ulofuranoside is often used in organic synthesis and as an intermediate in the preparation of various pharmaceuticals and other chemical products. Its structure and properties make it a valuable tool in the field of carbohydrate chemistry, where it can be used to study the reactions and transformations of sugar molecules.

7598-49-4

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7598-49-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7598-49-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,9 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7598-49:
(6*7)+(5*5)+(4*9)+(3*8)+(2*4)+(1*9)=144
144 % 10 = 4
So 7598-49-4 is a valid CAS Registry Number.

7598-49-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [3,4-diacetyloxy-5-(acetyloxymethyl)-5-ethoxyoxolan-2-yl]methyl acetate

1.2 Other means of identification

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Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

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More Details:7598-49-4 SDS

7598-49-4Downstream Products

7598-49-4Relevant academic research and scientific papers

Reaction of D-fructose, D-glucose and inulin with alcohols in the presence of iodine; a novel glycosidation procedure

Verhart, Cor G.J.,Fransen, Carel T.M.,Zwanenburg, Binne,Chittenden, Gordon J.F.

, p. 133 - 139 (2007/10/03)

An efficient procedure for the glycosidation of D-fructose and D-glucose catalyzed by iodine is described. The reaction yields mainly alkyl glycofuranosides. Treatment of inulin under similar conditions leads to inter-glycosidic bond cleavage and to formation of alkyl D-fructofuranosides. The reaction conditions are particularly mild and relatively selective.

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