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6-O-acetyl-2,3,4-tri-O-benzyl-α-D-galactopyranosyl bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61236-82-6

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61236-82-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61236-82-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,2,3 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 61236-82:
(7*6)+(6*1)+(5*2)+(4*3)+(3*6)+(2*8)+(1*2)=106
106 % 10 = 6
So 61236-82-6 is a valid CAS Registry Number.

61236-82-6Relevant articles and documents

Total Synthesis of Alvaradoins e and F, Uveoside, and 10-epi-Uveoside

Ng, Kevin,Shaktah, Ryan,Vardanyan, Laura,Minehan, Thomas G.

, p. 9175 - 9178 (2019)

Concise total syntheses of the anthracenone C-glycosides alvaradoins E and F, uveoside, and 10-epi-uveoside (1-4) have been accomplished from chrysophanic acid 8 and bromosugar 9. Key steps in the syntheses include the DBU-induced coupling of 8 and 9 to p

Synthesis of cis-(1 → 3)-glycosides of allyl 2-acetamido-4,6-O- benzylidene-2-deoxy-α-D-glucopyranoside

Madaj, Janusz,Jankowska, Magdalena,Wisniewski, Andrzej

, p. 1293 - 1300 (2007/10/03)

Syntheses of allyl 2,3,4-tri-O-benzyl-α-D-gluco- and D-galactopyranosyluronate-(1→3)-2-acetamido-4,6-O-benzylidene-2-deoxy- α-D-glucopyranoside via oxidation of the hydroxymethyl group of allyl 2,3,4-tri-O-benzyl-α-D-gluco- and D-galactopyranosyl-(1→3)-2-

Synthesis of hexasaccharide fragments of pectin

Clausen, Mads H.,Madsen, Robert

, p. 3821 - 3832 (2007/10/03)

Abstract: Short syntheses of partially methyl-esterified hexagalacturonates 1-5 are described as part of the development of strategies for the preparation of larger pectic oligosaccharides. The methodology is based on the repeated coupling of galactose mo

Synthesis of the pentasaccharide chain of the Forsman antigen

Paulsen,Buensch

, p. 143 - 167 (2007/10/02)

The pentasaccharide chain of the Forssman antigen, O-(2-acetamido-2-deoxy-alpha-D-galactopyranosyl)-(1 leads to 3)-O-(2-acetamido-2-deoxy-beta-D-galactopyranosyl)-(1 leads to 3)-O-alpha-D-galactopyranosyl-(1 leads to 4)-O-beta-D-galactopyranosyl-(1 leads

Bausteine von Oligosacchariden, XXIX. Synthese des Trisaccharids aus N-Acetylglucosamin, Galactose und Rhamnose einer O-determinanten Kette von Escherichia coli. Abhaengigkeit der Stereoselektivitaet der α-Glycosidsynthese von der Reaktivitaet des Pyranos

Paulsen, Hans,Lockhoff, Oswald

, p. 3079 - 3101 (2007/10/02)

The mercury salt catalysed reaction of substituted α-D-galactosyl halides with the reactive 4-OH groups of the rhamnosides 18 and 19 were studied.The order of reactivity of the halides increases with the following substituents: O-acetyl O-glucosyl O-b

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