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147126-58-7

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147126-58-7 Usage

Chemical Properties

White to Off-White Solid

Uses

A nonionic detergent for the solubilization of membrane bound protein.

Check Digit Verification of cas no

The CAS Registry Mumber 147126-58-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,1,2 and 6 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 147126-58:
(8*1)+(7*4)+(6*7)+(5*1)+(4*2)+(3*6)+(2*5)+(1*8)=127
127 % 10 = 7
So 147126-58-7 is a valid CAS Registry Number.

147126-58-7SDS

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 Octyl-2-acetamido-2-deoxy-β-D-glucopyranoside

1.2 Other means of identification

Product number -
Other names OCTYL-2-ACETAMIDO-2-DEOXY-SS-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

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

More Details:147126-58-7 SDS

147126-58-7Downstream Products

147126-58-7Relevant articles and documents

Straightforward glycosylation of alcohols and amino acids mediated by ionic liquid

Monasson, Olivier,Sizun-Thomé, Gwena?lle,Lubin-Germain, Nadège,Uziel, Jacques,Augé, Jacques

scheme or table, p. 202 - 205 (2012/06/30)

Green glycosylation of functionalized alcohols and α-amino acids, using an ionic liquid as a recyclable solvent, was performed in one step directly from the unprotected monosaccharide under scandium triflate or ferric chloride catalysis. Pure α- and β-glycosides could be obtained after specific enzymatic hydrolysis.

Protecting group free glycosidations using p-toluenesulfonohydrazide donors

Gudmundsdottir, Anna V.,Nitz, Mark

supporting information; scheme or table, p. 3461 - 3463 (2009/04/16)

(Figure Presented) N-Glycopyranosylsulfonohydrazides are introduced as glycosyl donors for protecting group free synthesis of O-glycosides, glycosyl azides, and oxazolines. Mono- and disaccharides containing a reducing terminal N-acelylglucosamine residue were condensed with p-toluenesulfonylhydrazide to give the desired β-D-pyranose donors. These donors can be activated with NBS and then glycosidated with the desired alcohol or transformed to the oxazoline or glycosyl azide.

N-ACETYLGLUCOSAMINE DERIVATIVES AND USE THEREOF

-

Page/Page column 12, (2010/02/12)

The present invention relates to An N-acetylglucosamine derivative represented by the following formula (1), and a hyaluronic acid production promoting agent containing the same and a skin external preparation containing the same: wherein R1 is a hydrogen atom or an alkyl group having 2 to 18 carbon atoms; R2, R3, and R4 are hydrogen atoms or acyl groups having 2 to 18 carbon atoms and may be all the same or different from others; the steric structure at position 1 may be α or β; provided that R1, R2, R3, and R4 must not be all hydrogen atoms. It is intended to provide an easily available hyaluronic acid production promoting agent and a skin external preparation whereby the production of hyaluronic acid can be promoted in the skin and thus the skin can be maintained in a vital and moist state so that it is expected that the human skin can be prevented from age.

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