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811473-55-9

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811473-55-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 811473-55-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,1,4,7 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 811473-55:
(8*8)+(7*1)+(6*1)+(5*4)+(4*7)+(3*3)+(2*5)+(1*5)=149
149 % 10 = 9
So 811473-55-9 is a valid CAS Registry Number.

811473-55-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(azidomethyl)-3,5-bis(phenylmethoxy)benzene

1.2 Other means of identification

Product number -
Other names 3,5-dibenzyloxyphenyl-1-methylene azide

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:811473-55-9 SDS

811473-55-9Relevant articles and documents

Size-selective phase-transfer catalysis with interfacially cross-linked reverse micelles

Lee, Li-Chen,Zhao, Yan

supporting information; experimental part, p. 784 - 787 (2012/04/17)

Cross-linking of the reverse micelles (RMs) of a triallylammonium surfactant afforded organic nanoparticles with introverted cationic groups. The cross-linked reverse micelles catalyzed size-selective biphasic reaction between sodium azide and alkyl bromi

Thermally reversible dendronized step-polymers based on sequential Huisgen 1,3-dipolar cycloaddition and diels-alder "click" reactions

Polaske, Nathan W.,McGrath, Dominie V.,McElhanon, James R.

experimental part, p. 1270 - 1276 (2011/10/02)

Thermally labile dendronized AA-BB step polymers are described. First through third generation dendritic bisfuran monomers 6a-6c were prepared in part by the Cu(I)-catalyzed azide-alkyne Huisgen 1,3-dipolar cycloaddition reaction and in turn polymerized b

METHOD OF USING CLICK CHEMISTRY TO FUNCTIONALIZE DENDRIMERS

-

Page/Page column 23, (2008/06/13)

A library of functionalized dendritic macromolecules was prepared in extremely high yields using no protecting group strategies and with only minimal purification steps through the use of copper(l)-catalyzed 1 ,3-dipolar cycloaddition of azides and termin

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