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7396-77-2

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7396-77-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7396-77-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,9 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7396-77:
(6*7)+(5*3)+(4*9)+(3*6)+(2*7)+(1*7)=132
132 % 10 = 2
So 7396-77-2 is a valid CAS Registry Number.

7396-77-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N'-(1,2-ethylene)-bis(3-methoxysalicylideneimine)

1.2 Other means of identification

Product number -
Other names N,N'-bis(2-hydroxyl-3-methoxybenzylidene)ethylenediamine

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:7396-77-2 SDS

7396-77-2Relevant articles and documents

Formation of polynuclear copper(II)-sodium(I) heterometallic complexes derived from salen-type Schiff bases

Bhowmik, Prasanta,Harms, Klaus,Chattopadhyay, Shouvik

, p. 113 - 120 (2013)

Three heteronuclear Cu(II)/Na(I) complexes, [Cu2(salen) 2Na(ClO4)(CH3CN)] (1) [Cu2(vanen) 2Na2(μ1,1-NCS)2] (2) and [(Cu)2(L)2(Na)

Selective targeting of synthetic antioxidants to mitochondria: Towards a mitochondrial medicine for neurodegenerative diseases?

Dessolin, Jean,Schuler, Marie,Quinart, Alice,De Giorgi, Francesca,Ghosez, Leon,Ichas, Fran?ois

, p. 155 - 161 (2002)

Mitochondria are the major source of superoxide, and are responsible for activating apoptosis and oxidative damage during acute neuronal cell death and neurodegenerative disorders like Alzheimer and Parkinson diseases. While the molecular mechanisms by wh

Controllable bulk solvent-free melt ring-opening polymerization (ROP) of l-lactide catalyzed by Ni(II) and Ni(II)-Ln(III) complexes based on the Salen-type Schiff-base ligand

Jin, Wen-Juan,Ding, Li-Qin,Chu, Zeng,Chen, Lei-Lei,Lü, Xing-Qiang,Zheng, Xiao-Yan,Song, Ji-Rong,Fan, Dai-Di

, p. 25 - 32 (2011)

A monometallic (Ni2+, 1) and a series of bimetallic (Ni 2+-Ln3+, Ln = Ce (2); Ln = Nd (3); Ln = Sm (4); Ln = Eu (5); Ln = Tb (6); Ln = Ho (7); Ln = Tm (8)) complexes based on the Salen-type Schiff-base ligand H2

On new solvatomorphs of the metalloligand [Ni(o-van-en)]

?ernák, Juraj,Falvello, Larry R.,Titi?, Ján,Tomás, Milagros,Vráblová, Anna

, (2020)

The Schiff-base bis-(2-hydroxy-3-methoxybenzylidene)ethylenediamine, denoted H2(o-van-en), is a versatile two-compartment polydentate ligand that can bring different guests, such as a transition metal and a lanthanoid, into close proximity to p

Bulk solvent-free melt ring-opening polymerization of L-lactide catalyzed by Cu(II) and Cu(II)-Nd(III) complexes of the Salen-type Schiff-base ligand

Chen, Lei-Lei,Ding, Li-Qin,Zeng, Chu,Long, Yong,Lue, Xing-Qiang,Song, Ji-Rong,Fan, Dai-Di,Jin, Wen-Juan

, p. 310 - 316 (2011)

A monometallic (Cu2+, 1) and a bimetallic (Cu 2+-Nd3+, 2) Salen-type Schiff-base complexes with different reactive species, could efficiently catalyze the bulk solvent-free melt ring-opening polymerization (ROP) of L-lacti

[RuIII(valen)(CN)2]-: A New Building Block to Design 4d-4f Heterometallic Complexes

Marinescu, Gabriela,Maxim, Catalin,Clérac, Rodolphe,Andruh, Marius

, p. 5621 - 5623 (2015)

New 4d-4f heterometallic complexes with a one-dimensional structure, 1∞[{Ru(valen)(CN)2KRu(valen)(CN)2}{Ln(O2NO)2(CH3OH)3}]·2CH3OH (Ln = Gd, Tb, Dy), have b

Syntheses of the Carotane-type Terpenoids (+)-Schisanwilsonene A and (+)-Tormesol via a Two-Stage Approach

Chen, Kai-Yue,Mou, Shu-Bin,Wang, Hua-Qi,Xiang, Zheng,Xiao, Wen

supporting information, p. 400 - 404 (2021/01/13)

Stereoselective syntheses of terpenoids in a more efficient manner have been a long-term pursuit for synthetic chemists. Herein we describe the two-step, enantiospecific and protecting-group-free synthesis of (+)-schisanwilsonene A from a carotane compound, which was produced in E. coli. We also completed the first enantiomeric synthesis of (+)-tormesol in five steps. The two-stage strategy offers a step- and redox-economical approach to prepare terpene natural products and their analogues.

Solvent-Dependent Bending Ability of Salen-Derived Organic Crystals

Kusumoto, Sotaro,Saso, Akira,Ohmagari, Hitomi,Hasegawa, Miki,Kim, Yang,Nakamura, Masaaki,Lindoy, Leonard F.,Hayami, Shinya

, p. 1692 - 1696 (2020/07/04)

The formation of plastic or brittle organic crystals of salen derivatives that depend on the solvents employed for crystallization is demonstrated. Large yellow crystals (ranging from mm to cm size) of ten different salen derivatives were obtained and inv

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