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1,4,7,10-Tetraoxa-13,16-diazacyclooctadecane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75173-44-3

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75173-44-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75173-44-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,1,7 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 75173-44:
(7*7)+(6*5)+(5*1)+(4*7)+(3*3)+(2*4)+(1*4)=133
133 % 10 = 3
So 75173-44-3 is a valid CAS Registry Number.

75173-44-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4,7,10-tetraoxa-13,16-diazacyclooctadecane

1.2 Other means of identification

Product number -
Other names -

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:75173-44-3 SDS

75173-44-3Downstream Products

75173-44-3Relevant academic research and scientific papers

Potentiometric and AM1d studies of the equilibria between silver(I) and diaza-15-crown and diaza-18-crown ethers with nitrogen in different positions in various solvents

Kira, Jaromir,Niedzialkowski, Pawel,Ossowski, Tadeusz

, p. 180 - 190 (2013/11/19)

Complex formation and stability constants between typical and atypical diaza-15-crown and diaza-18-crown ethers with silver(I) were determined in methanol, acetonitrile and propylene carbonate by the potentiometric method. In two of the diaza crown ethers, AA-diaza-15 and AA-diaza-18-crown, two nitrogens in the macrocyclic ring replaced two consecutive oxygens instead of two opposite ones in the two other diaza crown ethers. It was found that complexes of 1:1 and 1:2 metal-to-ligand stoichiometry were formed. The solvent composition and cavity size of crown ethers significantly influences the stability constants of complexes. AA-diaza-15 and AA-diaza-18-crown ethers were examined for comparison with diaza-15-crown and diaza-18-crown ethers. AA-diaza crown ethers formed less stable 1:1 metal-to-ligand complexes with silver(I) than typical diaza crown ethers but their ability to form 1:2 metal-to-ligand complexes was stronger. The energetically most favorable structures of the 1:1 metal-to-ligand complexes were calculated and visualized by the AM1d method at the semiempirical level of theory.

SYNTHESIS OF N-UNSUBSTITUTED DI- AND TRIAZA CROWN ETHERS.

Maeda,Furuyoshi,Nakatsuji,Okahara

, p. 3073 - 3077 (2007/10/02)

Facile syntheses of di- and triaza crown ethers by intramolecular cyclization of oligoethylene glycols containing two or three imino groups or by their intermolecular cyclization with oligoethylene glycol bis(p-toluenesulfonate)s are described.

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