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BIS(2-AMINOETHYL) ETHER N,N,N',N'-TETRAACETIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

923-73-9

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923-73-9 Usage

Purification Methods

Crystallise it from EtOH.

Check Digit Verification of cas no

The CAS Registry Mumber 923-73-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,2 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 923-73:
(5*9)+(4*2)+(3*3)+(2*7)+(1*3)=79
79 % 10 = 9
So 923-73-9 is a valid CAS Registry Number.

923-73-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-[2-[bis(carboxymethyl)amino]ethoxy]ethyl-(carboxymethyl)amino]acetic acid

1.2 Other means of identification

Product number -
Other names 2,2'-oxybis(ethylamine)-N,N,N',N'-tetraacetic acid

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:923-73-9 SDS

923-73-9Downstream Products

923-73-9Relevant academic research and scientific papers

Dendritic bis- and tetrakis-iminodiacetic acid-boronate complexes in one-pot cross-coupling reactions

Sharma, Anindra,Kumar, Prabhat,Pal, Rita,Jayaraman, Narayanaswamy

, p. 138 - 146 (2016)

Iminodiacetic acids are versatile metal chelating ligands. We herein undertook a study of dendritic bis- and tetrakis-iminodiacetic acids functionalized at the peripheries of branched core moieties. The dendritic iminodiacetic acids are synthesized by O- and N-alkylations of chosen alcohol and amine reactive sites emanating from a branched core. In order to identify the reactivities of such dendritic iminodiacetic acids, chelation with arylboronates is conducted. An assessment of the hydrolysis under aq. basic condition shows that dendritic boronates hydrolyze to boronic acid significantly slower than monomeric boronates. Slower hydrolysis of dendritic boronates is taken advantage, in order to conduct competitive [Formula presented] bond-forming Suzuki-Miyaura cross-coupling reactions. Teraryl synthesis is performed using monomeric and dendritic boronates. The iterative, multiple aryl-aryl bond formation is conducted subsequently, so as to prepare tetraaryls, through consecutive reactions of chosen boronic acid, monomeric boronate, dendritic boronate and aryl bromide, in one-pot. The study shows that slower hydrolysis of dendritic boronate is valuable in order to conduct multiple consecutive aryl-aryl bond formation.

Lower ligand denticity leading to improved thermodynamic and kinetic stability of the Gd3+ complex: The strange case of OBETA

Baranyai, Zsolt,Botta, Mauro,Fekete, Marianna,Giovenzana, Giovanni B.,Negri, Roberto,Tei, Lorenzo,Platas-Iglesias, Carlos

experimental part, p. 7680 - 7685 (2012/09/25)

OBETA, OBETA, you bet: Thermodynamic and kinetic measurements show an apparent paradox. The stability of complexes of lanthanide trivalent ions is higher with the heptadentate ligand OBETA (ethylene glycol-bis(2-aminoethyl ether)-N,N,N',N'-tetraacetic aci

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