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D,L-oliose, also known as 2-O-Methyl-L-Fucose or D,L-Fucose Methyl Ester, is a chemical compound derived from L-fucose, a naturally occurring sugar molecule. It has been studied for its potential biological activities, such as inhibiting bacterial adhesion to human cells, which could be useful in preventing bacterial infections. Additionally, D,L-oliose has been investigated for its potential as a therapeutic agent for certain inflammatory and autoimmune diseases, as well as for promoting the growth of beneficial bacteria in the gut, which could improve gut health and overall wellness.

4432-93-3

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4432-93-3 Usage

Uses

Used in Pharmaceutical Industry:
D,L-oliose is used as a potential therapeutic agent for inflammatory and autoimmune diseases due to its biological activities.
Used in Gut Health Applications:
D,L-oliose is used as a prebiotic to promote the growth of beneficial bacteria in the gut, contributing to improved gut health and overall wellness.
Used in Infection Prevention:
D,L-oliose is used to inhibit the adhesion of bacteria to human cells, which could help prevent bacterial infections.

Check Digit Verification of cas no

The CAS Registry Mumber 4432-93-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,3 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4432-93:
(6*4)+(5*4)+(4*3)+(3*2)+(2*9)+(1*3)=83
83 % 10 = 3
So 4432-93-3 is a valid CAS Registry Number.

4432-93-3Downstream Products

4432-93-3Relevant 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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