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Lyxo-hexose, 2,6-dideoxy- is a type of sugar molecule belonging to the family of deoxyhexoses, which are hexose sugars with one or more hydroxyl groups replaced by hydrogen atoms. This specific compound is characterized by the absence of hydroxyl groups at the 2nd and 6th carbon positions, making it a 2,6-dideoxy sugar. Lyxo-hexose, 2,6-dideoxy- is an important component in various biological processes, as it serves as a building block for the synthesis of certain antibiotics and other bioactive compounds. Its unique structure also plays a role in the development of new drugs targeting specific enzymes or receptors in the human body. In summary, lyxo-hexose, 2,6-dideoxy- is a significant deoxyhexose sugar with potential applications in medicine and pharmaceutical research.

5658-09-3

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5658-09-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5658-09-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,5 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5658-09:
(6*5)+(5*6)+(4*5)+(3*8)+(2*0)+(1*9)=113
113 % 10 = 3
So 5658-09-3 is a valid CAS Registry Number.

5658-09-3Downstream Products

5658-09-3Relevant academic research and scientific papers

Anthraquinone glycosides from marine Streptomyces sp. strain

Lu, Yuanyuan,Xing, Yingying,Chen, Chen,Lu, Jiansheng,Ma, Yihua,Xi, Tao

body text, p. 459 - 462 (2012/10/08)

Two new anthraquinone glycosides Strepnoneside A (1) and Strepnoneside B (2), together with Chromomycin A3 (3), were isolated from cultures of the marine Streptomyces sp. strain. The structures were elucidated on the basis of NMR spectroscopic and mass spectrometry data. Compound 3 exhibited cytotoxic activities against HCT 116 cell lines (IC50 = 300 ± 11 pM).

SILYL NITRONATES AND NITRILE OXIDES IN ORGANIC SYNTHESIS. A NOVEL ROUTE TO D,L-DEOXYSUGARS. USE OF ALUMINIUM OXIDE AS SOLID PHASE BASE FOR GENERATION OF NITRILE OXIDES FROM HYDROXIMIC ACID CHLORIDES

Torssell, K. B. G.,Hazell, A. C.,Hazell, R. G.

, p. 5569 - 5576 (2007/10/02)

Novel methodology is developed for a three step synthesis of deoxyaldoses and deoxyketoses. 1.Regioselective addition of silyl nitronate or nitrile oxide to a diene. 2.Stereospecific hydroxylation of the double bond. 3.Unmasking of the aldol moiety by catalytic reduction of the 2-isoxazoline.The syntheses of D.L-deoxyribose, D,L-oleose, D,L-digitoxose, D,L-2-deoxygalactose, 1,3-dideoxyfructose, 3-deoxyfructose etc. are described.Basic aluminium oxide is introduced as a solid phase base for the one step synthesis of 2-isoxazolines from aldoximes and olefins.An X-ray diffraction study of compound 13c verifies the stereochemical assignments.

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