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2-hydroxy-N-[2-((2-[(2-hydroxybenzoyl)amino]ethyl)amino)ethyl]benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76218-93-4

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76218-93-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76218-93-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,2,1 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 76218-93:
(7*7)+(6*6)+(5*2)+(4*1)+(3*8)+(2*9)+(1*3)=144
144 % 10 = 4
So 76218-93-4 is a valid CAS Registry Number.

76218-93-4SDS

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 N,N'-(azanediylbis(ethane-2,1-diyl))bis(2-hydroxybenzamide)

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:76218-93-4 SDS

76218-93-4Relevant academic research and scientific papers

Proximity effect on the general base catalysed hydrolysis of amide linkage: The role of cationic surfactant, CTABr

Dash, Sarat C.,Dash, Anadi C.

, p. 497 - 507 (2011)

The bis phenoxide forms of (1,2) bis(2-hydroxybenzamido) ethane(I) , (1,5) bis(2-hydroxybenzamido) 3-azapentane(II) , (1,3) bis(2-hydroxybenzamido) propane(III) , and (1,8) bis(2-hydroxybenzamido) 3,6- diazaoctane(IV) undergo facile hydrolysis of one of the amide groups (0.02 ≤ [OH?]T (mol dm? 3) ≤ 0.5, 10% MeOH (v/v) + H2O medium) without exhibiting [OH?] dependence. The reactivity trend follows I ~ II >> III ~ IV with low activation enthalpy {25.7±2.8 ≤ δH≠ (kJ mol?1) ≤ 64.8±7.0}. The high negative and comparable values of activation entropy{?234 ±8 ≤ δS≠ (J K?1 mol? 1) ≤ ?127 ± 20} are consistent with closely similar, and ordered transition states which can be assembled by favourably oriented phenoxide groups. The solvent kinetic isotope effect for I, κ H2O/κ D2O+H2O ~ 1 (20 and 50 volume% D2O) , indicates that proton transfer is not involved as a part of the rate controlling process. The observed slowing down of the rate of this reaction for I in the micellar pseudo phase of CTABr also supports the proposed mechanism. Under premicellar conditions, however, rate acceleration is observed, a consequence believed to be associated with the capping effect of the hydrophobic tail of the surfactant cation forming the reactive ion-pair, CTA+, (I-2H) 2? exclusively in the aqueous pseudo phase. Indian Academy of Sciences.

A zwitterion of 1,5-bis(2-hydroxybenzamido)-3-azapentane: A two-dimensional hydrogen-bonding network involving dimers

Liu, Hui-Min,He, Lei,Luo, Xiao-Lan,Zhang, Wen-Qin

, p. o104-o106 (2006)

The title compound, 2-{N-[2-(2-hydroxybenzamido)ethylammonioethyl] aminocarbonyl}phenolate, C18H21N3O4, crystallizes in a zwitterionic form as a result of intermolecular proton transfer and possesses a negativel

Studies on some diamide copper (II) complexes

Sureshan,Bhattacharya

, p. 723 - 726 (2007/10/03)

Two diamides 1,5-bis (2-hydroxybenzamido)-4-azo-pentane (H2L) and 1,7- bis(2-hydroxybenzamido)-4-azo-heptane (H2L), which can act both as mononucleating and binucleating ligands, have been synthesised. Mononuclear LCu.H2O

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