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3,4,5-tris-benzoyloxy-6-{3-benzoyloxy-2-[3-benzoyloxy-5-hydroxy-2-(4-methoxy-phenoxy)-6-sulfooxymethyl-tetrahydro-pyran-4-yloxy]-5-hydroxy-6-sulfooxymethyl-tetrahydro-pyran-4-yloxy}-tetrahydro-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.

744196-54-1

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744196-54-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 744196-54-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,4,1,9 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 744196-54:
(8*7)+(7*4)+(6*4)+(5*1)+(4*9)+(3*6)+(2*5)+(1*4)=181
181 % 10 = 1
So 744196-54-1 is a valid CAS Registry Number.

744196-54-1Downstream Products

744196-54-1Relevant academic research and scientific papers

Synthesis of various sulfoforms of the trisaccharide β-D-GlcpA-(1→3)-β-D-Galp-(1→3)-β-D-Galp-(1→OMP) as probes for the study of the biosynthesis and sorting of proteoglycans

Thollas, Bertrand,Jacquinet, Jean-Claude

, p. 434 - 442 (2007/10/03)

A straightforward preparation of various sulfoforms of the trisaccharide 4-methoxyphenyl O-(sodium β-D-glucopyranosyluronate)-(1 → 3)-(β-D-galactopyranosyl)-(1 → 3)-β-D-galactopyranoside (1), namely its 6a- and 4a-monosulfate, 6b- and 4b-monosulfate and 6a,6b-disulfate derivatives, is reported/or the first time. These compounds, which are partial structures of the linkage region of proteoglycans, will serve as probes for the study of the biosynthesis and sorting of these macromolecules. A key trisaccharide derivative, in which the two similar D-Gal units were differentiated at C-4,6 with 4,6-benzylidene and 4,6-di-tert-butylsilylene acetals, respectively, was used as a common intermediate. Both acetal groups showed excellent orthogonality, and allowed the preparation of all target compounds in high yield. Noteworthy is the possibility to prepare the 6a- and 6b-monosulfated and the 6a,6b-disulfated species through a one-pot regioselective procedure starting from a tetrol precursor.

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