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1-(D-glucopyranosyl)piperidine is a chemical compound that consists of a piperidine ring, which is a six-membered nitrogen-containing ring, attached to a D-glucopyranosyl group. This D-glucopyranosyl group is a monosaccharide derived from glucose, with a pyranose ring structure. The compound is of interest in the field of organic chemistry and may have potential applications in pharmaceuticals or as a chiral building block due to its unique structure that combines a sugar moiety with a basic nitrogen-containing ring. It is important to note that the specific properties, reactivity, and applications of 1-(D-glucopyranosyl)piperidine would depend on its stereochemistry and the context in which it is used.

5017-79-8

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5017-79-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5017-79-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,1 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5017-79:
(6*5)+(5*0)+(4*1)+(3*7)+(2*7)+(1*9)=78
78 % 10 = 8
So 5017-79-8 is a valid CAS Registry Number.

5017-79-8SDS

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 (2R,3S,4S,5R)-2-(hydroxymethyl)-6-piperidin-1-yloxane-3,4,5-triol

1.2 Other means of identification

Product number -
Other names 1-Glucopyranosylpiperidine

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:5017-79-8 SDS

5017-79-8Downstream Products

5017-79-8Relevant academic research and scientific papers

Syntheses and structures of anomeric quaternary ammonium β-glucosides and comments on the anomeric C-N bond lengths

Iddon, Lisa,Bragg, Ryan A.,Harding, John R.,Pidathala, Chandrakala,Bacsa, John,Kirby, Anthony J.,Stachulski, Andrew V.

scheme or table, p. 6396 - 6402 (2009/12/09)

We report convenient syntheses of anomeric quaternary ammonium β-glucosides in both protected and deprotected forms, together with X-ray structural investigations of two of the products. Both the quaternisation of a protected anomeric N,N-(dimethylamino)g

Design and Synthesis of Mannose Analogues as Inhibitors of α-Mannosidase

Maity, Sanat K.,Dutta, Samir K.,Banerjee, Asish K.,Achari, Basudeb,Singh, Manoranjan

, p. 6965 - 6974 (2007/10/02)

A series of N-, C- and S- mannopyranosyl derivatives (4, 9-16) have been synthesised and their inhibitory activity tested towards jackbean α-mannosidase (EC 3.2.1.24).These compounds are of mechanistic and synthetic interest in the design of new α-mannosidase inhibitors.

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