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α-D-Xylo-4,6-dideoxy-hexopyranose is a monosaccharide, a type of sugar molecule, that is derived from the hexose sugar D-xylose. It is characterized by the absence of two hydroxyl groups, specifically at the 4th and 6th carbon positions, which is indicated by the term "dideoxy." This modification results in a unique structure that distinguishes it from its parent sugar. The "α" prefix denotes the anomeric configuration, which refers to the stereochemistry around the carbon atom that was originally at the reducing end of the sugar. This specific arrangement is important in determining how the sugar will interact with other molecules in biological systems. α-D-Xylo-4,6-dideoxy-hexopyranose is found in certain natural products and can be a component of more complex carbohydrates. Its unique structure may also have implications for its reactivity and potential applications in chemistry and biology.

22435-60-5

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22435-60-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22435-60-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,4,3 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 22435-60:
(7*2)+(6*2)+(5*4)+(4*3)+(3*5)+(2*6)+(1*0)=85
85 % 10 = 5
So 22435-60-5 is a valid CAS Registry Number.

22435-60-5Relevant academic research and scientific papers

Synthesis and Structural Characteristics of all Mono- And Difluorinated 4,6-Dideoxy- d - Xylo-hexopyranoses

Briggs, Edward L.,Fontenelle, Clement Q.,Kuppala, Ramakrishna,Light, Mark E.,Linclau, Bruno,Szpera, Robert,Vendeville, Jean-Baptiste,Wells, Neil J.,Wheatley, David E.

, p. 7725 - 7756 (2021/06/28)

Protein-carbohydrate interactions are implicated in many biochemical/biological processes that are fundamental to life and to human health. Fluorinated carbohydrate analogues play an important role in the study of these interactions and find application a

Sugar-Pirating as an Enabling Platform for the Synthesis of 4,6-Dideoxyhexoses

Zhang, Yinan,Zhang, Jianjun,Ponomareva, Larissa V.,Cui, Zheng,Van Lanen, Steven G.,Thorson, Jon S.,Thorson, Jon S.

supporting information, p. 9389 - 9395 (2020/06/27)

An efficient divergent synthetic strategy that leverages the natural product spectinomycin to access uniquely functionalized monosaccharides is described. Stereoselective 2′- and 3′-reduction of key spectinomycin-derived intermediates enabled facile acces

Synthesis of 4-deoxy and 4-deoxy-4-halogeno derivatives of L-fucose as potential enzyme inhibitors

Lindhorst, Thisbe K.,Thiem, Joachim

, p. 119 - 129 (2007/10/02)

Methyl-2,3-di-O-benzoyl-6-deoxy-α-L-galactopyranoside (2) was converted into the 4-deoxy-4-iodo-α-L-gluco derivative 4 by triflate-mediated inversion.Catalytic reduction of 4 gave methyl 2,3-di-O-benzoyl-4,6-dideoxy-α-L-xylo-hexopyranoside (6) and subsequ

Formal total synthesis of grahamimycin A1

Ohta,Mitsunobu

, p. 517 - 520 (2007/10/02)

(S)-t-Butyldimethylsiloxy-2-hexenoic acid and its (R)-isomer were prepared from (S)- and (R)-3-hydroxybutanoic acid esters, respectively. Condensation of the both isomers with 2-(p-toluenesulfonyl)ethyl (4S,5S,7R)-7-hydroxy-4,5-dimethylmethylenedioxyoctan

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