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3947-62-4

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  • China Biggest Factory Manufacturer 2,3,4,6-Tetra-o-acetyl-D-glucopyranose CAS 3947-62-4

    Cas No: 3947-62-4

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3947-62-4 Usage

Uses

2,3,4,6-Tetra-O-acetyl-D-glucopyranose can be used as a catalyst.

Check Digit Verification of cas no

The CAS Registry Mumber 3947-62-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,4 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3947-62:
(6*3)+(5*9)+(4*4)+(3*7)+(2*6)+(1*2)=114
114 % 10 = 4
So 3947-62-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H20O10/c1-6(15)20-5-10-11(21-7(2)16)12(22-8(3)17)13(14(19)24-10)23-9(4)18/h10-14,19H,5H2,1-4H3/t10-,11-,12+,13-,14-/m1/s1

3947-62-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,4,6-Tetra-O-acetyl-β-D-glucose

1.2 Other means of identification

Product number -
Other names 2,3,4,6-tetra-O-acetyl-glucopyranose

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:3947-62-4 SDS

3947-62-4Relevant articles and documents

Chromatographic procedures for isolating α,β-trehalose formed during the preparation of β,β-trehalose

Parrish, Frederick W.,Meagher, Michael M.,Reilly, Peter J.

, p. 129 - 135 (1987)

-

Controlled In-Cell Generation of Active Palladium(0) Species for Bioorthogonal Decaging

Bernardes, Gon?alo J. L.,Day, Jason,Domingos, Josiel B.,Jiménez-Moreno, Ester,Kon?, Juraj,Latocheski, Eloah,Pérez, Laura Rodríguez,Sabatino, Valerio

supporting information, (2022/01/11)

Owing to their bioorthogonality, transition metals have become very popular in the development of biocompatible bond-cleavage reactions. However, many approaches require design and synthesis of complex ligands or formulation of nanoparticles which often perform poorly in living cells. This work reports on a method for the generation of an active palladium species that triggers bond-cleaving reactions inside living cells. We utilized the water-soluble Na2PdCl4 as a simple source of PdII which can be intracellularly reduced by sodium ascorbate to the active Pd0 species. Once generated, Pd0 triggers the cleavage of allyl ether and carbamate caging groups leading to the release of biologically active molecules. These findings do not only expand the toolbox of available bioorthogonal dissociative reactions but also provide an additional strategy for controlling the reactivity of Pd species involved in Pd-mediated bioorthogonal reactions.

An alternative approach for the synthesis of sulfoquinovosyldiacylglycerol

Domey, Hendrik,Fischer, Judith,Rohn, Sascha,Sitz, Tobias

, (2021/07/28)

Sulfoquinovosyldiacylglycerol (SQDG) is a glycolipid ubiquitously found in photosyn-thetically active organisms. It has attracted much attention in recent years due to its biological ac-tivities. Similarly, the increasing demand for vegan and functional foods has led to a growing interest in micronutrients such as sulfolipids and their physiological influence on human health. To study this influence, reference materials are needed for developing new analytical methods and providing enough material for model studies on the biological activity. However, the availability of these materials is limited by the difficulty to isolate and purify sulfolipids from natural sources and the unavailability of chemical standards on the market. Consequently, an alternative synthetic route for the comprehensive preparation of sulfolipids was established. Here, the synthesis of a sulfolipid with two identical saturated fatty acids is described exemplarily. The method opens possibilities for the preparation of a diverse range of interesting derivatives with different saturated and unsatu-rated fatty acids.

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