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Benzoic acid (2S,3R,4S,5R,6R)-4,5-dihydroxy-6-hydroxymethyl-2-(4-methoxy-phenoxy)-tetrahydro-pyran-3-yl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

904684-24-8

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904684-24-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 904684-24-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,4,6,8 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 904684-24:
(8*9)+(7*0)+(6*4)+(5*6)+(4*8)+(3*4)+(2*2)+(1*4)=178
178 % 10 = 8
So 904684-24-8 is a valid CAS Registry Number.

904684-24-8Relevant academic research and scientific papers

Synthesis of a set of sulfated and/or phosphorylated oligosaccharide derivatives from the carbohydrate-protein linkage region of proteoglycans

Jacquinet, Jean-Claude

, p. 1630 - 1644 (2007/10/03)

The synthesis of a set of various sulfoforms and/or phosphoforms as 7-methoxy-2-naphthyl glycosides of β-d-Xylp, β-d-Galp-(1→4)-β-d-Xylp, and β-d-Galp-(1→3)-β-d-Galp-(1→4)-β-d-Xylp, structures encountered in the common carbohydrate-protein linkage region

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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