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129575-89-9

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  • 4-Methoxyphenyl 3,6-Di-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside

    Cas No: 129575-89-9

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  • 2-[(2S,3R,4R,5S,6R)-5-hydroxy-2-(4-methoxyphenoxy)-4-phenylmethoxy-6-(phenylmethoxymethyl)oxan-3-yl]isoindole-1,3-dione

    Cas No: 129575-89-9

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129575-89-9 Usage

Uses

4-Methoxyphenyl 3,6-Di-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside (CAS# 129575-89-9) is a useful glycoside building block used in the synthesis of glycans.

Check Digit Verification of cas no

The CAS Registry Mumber 129575-89-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,5,7 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 129575-89:
(8*1)+(7*2)+(6*9)+(5*5)+(4*7)+(3*5)+(2*8)+(1*9)=169
169 % 10 = 9
So 129575-89-9 is a valid CAS Registry Number.
InChI:InChI=1/C35H33NO8/c1-40-25-16-18-26(19-17-25)43-35-30(36-33(38)27-14-8-9-15-28(27)34(36)39)32(42-21-24-12-6-3-7-13-24)31(37)29(44-35)22-41-20-23-10-4-2-5-11-23/h2-19,29-32,35,37H,20-22H2,1H3/t29-,30-,31-,32-,35-/m1/s1

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  • TCI America

  • (M1615)  4-Methoxyphenyl 3,6-Di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside  >95.0%(HPLC)

  • 129575-89-9

  • 1g

  • 1,890.00CNY

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129575-89-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2S,3R,4R,5S,6R)-5-hydroxy-2-(4-methoxyphenoxy)-4-phenylmethoxy-6-(phenylmethoxymethyl)oxan-3-yl]isoindole-1,3-dione

1.2 Other means of identification

Product number -
Other names 4-Methoxyphenyl 3,6-Di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:129575-89-9 SDS

129575-89-9Downstream Products

129575-89-9Relevant articles and documents

Synthesis of glycosyl acceptors by regioselective benzylations of a 2-deoxy-2-phthalimido-D-glucoside

Robina, Inmaculada,Lopez-Barba, Eugenia,Fuentes, Jose

, p. 2847 - 2856 (1996)

The direct regioselective benzylation of p-methoxyphenyl 2-deoxy-2-phthalimido-β-D-glucopyranoside (1) with benzyl bromide under basic conditions gives 4,6-di-O-benzyl (2a), 4-O-benzyl (3a) and 6-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 4a. When

Chemoenzymatic approach for the preparation of asymmetric bi-, tri-, and tetra-antennary N-glycans from a common precursor

Gagarinov, Ivan A.,Li, Tiehai,Tora?o, Javier Sastre,Caval, Tomislav,Srivastava, Apoorva D.,Kruijtzer, John A. W.,Heck, Albert J. R.,Boons, Geert-Jan

, p. 1011 - 1018 (2017/05/16)

Progress in glycoscience is hampered by a lack of well-defined complex oligosaccharide standards that are needed to fabricate the next generation of microarrays, to develop analytical protocols to determine exact structures of isolated glycans, and to elu

Use of methanesulfonic acid in the reductive ring-opening of O-benzylidene acetals

Zinin, Alexander I.,Malysheva, Nelly N.,Shpirt, Anna M.,Torgov, Vladimir I.,Kononov, Leonid O.

, p. 627 - 630 (2008/03/13)

Methanesulfonic acid was shown to be an efficient and convenient substitute for ethereal HCl in reductive 4,6-O-benzylidene acetal ring-opening reaction with sodium cyanoborohydride in THF. Normal regioselectivity was observed, the 6-O-benzyl ethers with

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