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1,2-Ethanediamine, N-[(2,4,6-trimethylphenyl)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

676473-67-9

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676473-67-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 676473-67-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,6,4,7 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 676473-67:
(8*6)+(7*7)+(6*6)+(5*4)+(4*7)+(3*3)+(2*6)+(1*7)=209
209 % 10 = 9
So 676473-67-9 is a valid CAS Registry Number.

676473-67-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-[(2,4,6-trimethylphenyl)methyl]ethane-1,2-diamine

1.2 Other means of identification

Product number -
Other names Trimethylbenzylaminoaethylamin

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:676473-67-9 SDS

676473-67-9Relevant academic research and scientific papers

A theoretical insight for solvent effect on myoglobin assay of W(CO)4L2 type novel complexes with DFT/TDDFT

üstün, Elvan,Demi?r, Serpil,Co?kun, Feyzullah,Kalo?lu, Murat,?ahi?n, Onur,Büyükgüng?r, Orhan,?zdemi?r, ?smail

, p. 433 - 440 (2016/07/25)

Novel tetracarbonyl complexes of type W(CO)4L2 (L: 4-chlorobenzylimidazoline; 4-methylbenzylimidazoline; 3,5-dimethylbenzylimidazoline; 2,4,6-trimethylbenzylimidazoline; 2,3,5,6- tetramethylbenzylimidazoline) were synthesized. Then n

First examples of carbene-catalyzed allylation of benzaldehyde with allyltrichlorosilane

Tabassum, Sobia,Gilani, Mazhar Amjad,Ayub, Khurshid,Wilhelm, René

, p. 1199 - 1205 (2015/06/02)

Abstract We report here first examples of carbene-catalyzed allylation of benzaldehyde. N-Heterocyclic carbenes applied here, 9a and 10a, were derived from imidazolinium zwitterions, and contained sulfonate and sulfamate substituents, respectively. Different reaction conditions such as temperature, organic solvents, additive and bases were used to optimize the reaction. Sulfonate substituted NHC 9a is found more efficient organocatalyst for the allyltion of benzaldehyde (greater than 99 % yield at lower temperature) than sulfamate-based NHC 10a (a yield of no more than 15 %). These results are justified on the basis of philicity descriptors of the NHCs and their corresponding allyldichlorosilane complexes. Graphical abstract: [Figure not available: see fulltext.]

Imidazolinium sulfonate and sulfamate zwitterions as chiral solvating agents for enantiomeric excess calculations

Tabassum, Sobia,Gilani, Mazhar Amjad,Wilhelm, Rene

, p. 1632 - 1639 (2012/01/04)

The synthesis of enantiopure unsymmetrical N-heterocyclic based zwitterions incorporating imidazolinium and alkylsulfonate or sulfamate groups is described. The desired compounds were prepared in good yields from 1,3-propanesultone or cyclic sulfamidates

Benzylic imidazolidinium, 3,4,5,6-tetrahydropyrimidinium and benzimidazolium salts: Applications in ruthenium-catalyzed allylic substitution reactions

Yasar, Sedat,Oezdemir, Ismail,Cetinkaya, Bekir,Renaud, Jean-Luc,Bruneau, Christian

experimental part, p. 2142 - 2149 (2009/04/04)

Imidazolidinium, tetrahydropyrimidinium and benzimidazolium salts were prepared. Upon reaction with tBuOK, they generate carbene ligands, which were associated in situ to [RuCp*(MeCN)3]PF6 to produce ruthenium catalysts that are acti

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