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(4S,5R,6R)-6-Benzyloxy-4,5-dihydroxy-5,6-dihydro-4H-pyran-2-carboxylic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71200-17-4

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71200-17-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71200-17-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,2,0 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 71200-17:
(7*7)+(6*1)+(5*2)+(4*0)+(3*0)+(2*1)+(1*7)=74
74 % 10 = 4
So 71200-17-4 is a valid CAS Registry Number.

71200-17-4Downstream Products

71200-17-4Relevant academic research and scientific papers

Conformational study of synthetic Δ4-uronate monosaccharides and glycosaminoglycan-derived disaccharides

Bazin, Helene G.,Capila, Ishan,Linhardt, Robert J.

, p. 135 - 144 (2007/10/03)

Sixteen Δ4-uronate monosaccharides were chemically synthesized. Their carboxy group was protected as a methyl or benzyl ester, the anomeric hydroxyl group as a benzyl glycoside and the 2 and 3 hydroxyl groups were protected with different substitution patterns as both ester and ether derivatives. Disaccharides containing Δ4-uronates were prepared from heparin using heparin lyases. Their carboxy group was unprotected or protected as a benzyl ester and the two hydroxyls in the uronate moiety were free, as O-sulfo derivatives or acylated. The conformation of these unsaturated uronate monosaccharide and disaccharide residues was studied using 1H NMR by examining interproton vic inal coupling constants. The Δ4-uronate residue adopted either the 2H1 or the 1H2 conformations. The equilibrium between these two conformers was shown to be controlled by substitution pattern.

Regio and stereoselective conversion of Δ4-uronic acids to L-ido- and D-glucopyranosiduronic acids

Bazin, Helene G.,Kerns, Robert J.,Linhardt, Robert J.

, p. 923 - 926 (2007/10/03)

Synthesis of L-ido- and D-glucopyranosiduronic acids was performed starting from protected Δ4-uronic acids 3a-f. Bromination of the C-4,5 double bond provided the trans-diaxial bromohydrin derivatives 6a-d, which were converted to the corresponding epoxides 7a-d in high yields. Direct reduction of these epoxides using borane-tetrahydrofuran complex afforded the D-glucopyranosiduronic acids 9b-d, while Lewis acid rearrangement through the C-4 keto intermediate 10b-d afforded the L-idopyranosiduronic acids 11b-d.

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