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132201-75-3

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132201-75-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132201-75-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,2,0 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 132201-75:
(8*1)+(7*3)+(6*2)+(5*2)+(4*0)+(3*1)+(2*7)+(1*5)=73
73 % 10 = 3
So 132201-75-3 is a valid CAS Registry Number.

132201-75-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name O-(2,3,4,6-tetra-O-benzyl-α,β-D-glucopyranosyl) trichloroacetimidate

1.2 Other means of identification

Product number -
Other names O-((2,3,4,6-tetra-O-benzyl)-D-glucopyranosyl)trichloroacetimidate

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:132201-75-3 SDS

132201-75-3Downstream Products

132201-75-3Relevant articles and documents

Decarboxylative glycosylation reaction - Intra- versus intermolecular reaction course

Scheffler, Goetz,Schmidt, Richard R.

, p. 2943 - 2946 (1997)

Mixed glycosyl carbonates are transformed under acid catalysis into glycosides. Competition experiments with equal amounts of carbonates 5 and 6 led to complete scrambling of the glycosyl donor and acceptor moieties: not only the expected glycosides 7 and

Stereoselective O-Glycosylations by Pyrylium Salt Organocatalysis**

Holmstr?m, Thomas,Nielsen, Michael Martin,Pedersen, Christian Marcus

supporting information, (2021/12/30)

Despite many years of invention, the field of carbohydrate chemistry remains rather inaccessible to non-specialists, which limits the scientific impact and reach of the discoveries made in the field. Aiming to increase the availability of stereoselective

Synthesis of nature product kinsenoside analogues with anti-inflammatory activity

Song, Wei,Sun, Yong,Xu, Lintao,Sun, Yajing,Li, Tianlu,Peng, Peng,Lou, Hongxiang

supporting information, (2020/12/02)

Kinsenoside is the major bioactive component from herbal medicine with a broad range of pharmacological functions. Goodyeroside A, an epimer of kinsenoside, remains less explored. In this report we chemically synthesized kinsenoside, goodyeroside A and their analogues with glycan variation, chirality inversion at chiral center(s), and bioisosteric replacement of lactone with lactam. Among these compounds, goodyeroside A and its mannosyl counterpart demonstrated superior anti-inflammatory efficacy. Furthermore, goodyeroside A was found to suppresses inflammatory through inhibiting NF-κB signal pathway, effectively. Structure-activity relationship is also explored for further development of more promising kinsenoside analogues as drug candidates.

Visible-Light-Mediated β-C(sp3)-H Amination of Glycosylimidates: En Route to Oxazoline-Fused/Spiro Nonclassical Bicyclic Sugars

Shaw, Mukta,Kumar, Amit

supporting information, (2019/05/08)

A straightforward route has been developed for the diastereoselective synthesis of nonclassical conformationally constrained oxazoline-fused and spiro bicyclic sugars bearing a quaternary center via selective β-C-H amination of appropriately positioned gl

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