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Benzenamine, 2,4,6-trimethyl-N-(1H-pyrrol-2-ylmethylene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

383889-16-5

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383889-16-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 383889-16-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,3,8,8 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 383889-16:
(8*3)+(7*8)+(6*3)+(5*8)+(4*8)+(3*9)+(2*1)+(1*6)=205
205 % 10 = 5
So 383889-16-5 is a valid CAS Registry Number.

383889-16-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-trimethyl-N-(pyrrol-2-ylidenemethyl)aniline

1.2 Other means of identification

Product number -
Other names 2-[(2,4,6-Me3C6H4)N=CH](C4H3NH)

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:383889-16-5 SDS

383889-16-5Relevant academic research and scientific papers

Synthesis, characterization and cancer cell growth inhibition activity of ruthenium(II) complexes bearing bidentate pyrrole-imine ligands

Chen, Guan-Hao,Leu, Wohn-Jenn,Guh, Jih-Hwa,Lin, Chia-Her,Huang, Jui-Hsien

, p. 122 - 130 (2018/05/28)

A series of bidentate pyrrole-imine ligands, [C4H3NH-(2-CH=N-R)] (1, R = cyclohexenyl; 2, R = CH2CH2-1-cyclohexenyl; 3, R = tBu; 4, R = CH2-2-furyl; 5, R = 2-methoxylphenyl; 6, R = phenyl;

Rare earth metal bis(trimethylsilyl)amido complexes bearing pyrrolyl-methylamide ligand. Synthesis, structure, and catalytic activity towards guanylation of amines

Liu, Chao,Zhou, Shuangliu,Wang, Shaowu,Zhang, Lijun,Yang, Gaosheng

experimental part, p. 8994 - 8999 (2011/01/08)

The N-arylaminomethyl substituted pyrrolyl ligand 2-[(2,4,6-Me 3C6H2)NHCH2](C4H 3NH) (1) was synthesized by reduction of 2-[(2,4,6-Me 3C6H2)NCH](C4H3NH) using NaBH4. Treatment of [(Me3Si)2N] 3Ln(μ-Cl)Li(THF)3 with 1 equiv. of 1 in reflux toluene for 24 h, afforded the corresponding trivalent rare earth metal amides with formula {(μ-η5:η1):η1-2-[(2,4,6- Me3C6H2)NCH2]C4H 3N]LnN(SiMe3)2}2 (Ln = Y(2), Nd(3), Sm(4), Dy(5), Er(6)). All compounds were fully characterised by spectroscopic methods and elemental analyses. The structures of complexes 2, 4 and 6 were determined by single-crystal X-ray analyses. X-Ray analyses discovered that two rare-earth metal ions were bridged by dianion ligand with the pyrrolyl ring which coordinated to one rare earth metal in an η5 mode, the tethered nitrogen anion and nitrogen atom of the pyrrolyl ring coordinated to another rare earth metal in η1 modes forming the centrosymmetric dinuclear structures. The rare earth metal complexes as catalysts for the guanylation of aromatic amines were studied. Results showed all rare earth metal complexes exhibited a high catalytic activity on the guanylation of aromatic amines. The Royal Society of Chemistry 2010.

Chelating N-pyrrolylphosphino-N′-arylaldimine ligands: Synthesis, ligand behaviour and applications in catalysis

Anderson, Carly E.,Batsanov, Andrei S.,Dyer, Philip W.,Fawcett, John,Howard, Judith A. K.

, p. 5362 - 5378 (2007/10/03)

Two families of variously-substituted N-pyrrolylphosphino-N′- arylaldimine ligands, 2-(aryl-NCH)C4H3N-PR2 {3a-d R = Ph; 4a-d R = Pri2N}, have been prepared from the corresponding pyrrolylaldimines 2.

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