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2-Hydroxyethyl 2-acetamido-2-deoxyhexopyranoside is a complex organic compound with the molecular formula C10H19NO6. It is a derivative of a hexopyranoside, which is a type of sugar molecule, and features a 2-hydroxyethyl group attached to the 2-position of the molecule. The acetamido group at the 2-position indicates the presence of an amide functional group derived from acetic acid. 2-hydroxyethyl 2-acetamido-2-deoxyhexopyranoside is of interest in the field of carbohydrate chemistry and may have applications in the synthesis of complex carbohydrates and related biologically active molecules. Its structure and properties make it a potential candidate for studying the interactions of sugars with proteins and other biomolecules, as well as for the development of new drugs and therapeutics that target carbohydrate-binding sites.

3055-52-5

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3055-52-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3055-52-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,5 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3055-52:
(6*3)+(5*0)+(4*5)+(3*5)+(2*5)+(1*2)=65
65 % 10 = 5
So 3055-52-5 is a valid CAS Registry Number.

3055-52-5Upstream product

3055-52-5Downstream Products

3055-52-5Relevant academic research and scientific papers

Effect of Treatment Methods on Chitin Structure and Its Transformation into Nitrogen-Containing Chemicals

Chen, Xi,Gao, Yongjun,Wang, Lan,Chen, Hongzhang,Yan, Ning

, p. 1565 - 1572 (2015)

Chitin treatment using different methods, including ball mill grinding, steam explosion, alkaline treatment, phosphoric acid, and ionic liquid (IL) dissolution/reprecipitation have been systematically investigated. The chitin structures were thoroughly investigated by using a series of analytical techniques, and the reactivity after each treatment was evaluated in dehydration and liquefaction reactions. The parallel studies enable direct comparisons of these methods and help to establish the structure-activity correlations. Ball mill grinding in dry mode was the most effective method, with the crystal size and the hydrogen-bond network being the two crucial factors in enhancing the reactivity. Remarkably, the yield of 3-acetamido-5-acetylfuran (3A5AF) from chitin dehydration increased to the highest amount (28.5%) after ball mill grinding (the previous record yield was 7.5% for untreated chitin).

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