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Benzenamine, N,N-dimethyl-4-[(1E,3E)-4-(4-pyridinyl)-1,3-butadienyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

222165-16-4

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222165-16-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 222165-16-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,2,1,6 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 222165-16:
(8*2)+(7*2)+(6*2)+(5*1)+(4*6)+(3*5)+(2*1)+(1*6)=94
94 % 10 = 4
So 222165-16-4 is a valid CAS Registry Number.

222165-16-4SDS

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-dimethyl-4-(4-pyridin-4-ylbuta-1,3-dienyl)aniline

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:222165-16-4 SDS

222165-16-4Relevant academic research and scientific papers

Amino substituted 4-pyridylbutadienes: Synthesis and fluorescence investigations

Agnihotri, Harsha,Mahalingavelar, Paramasivam,Mande, Hemant,Ghalsasi, Prasanna,Kanvah, Sriram

, p. 341 - 348 (2015/09/07)

Synthesis and spectroscopic investigations of a series of donor-π-acceptor systems containing pyridine as the electron withdrawing group and an amino derivative (dimethylamino, diphenylamino, carbazole and julolidine) as electron donating group, separated by a π-spacer are described. The effect of varying donors on absorption and emission properties was studied in different solvents. All the molecules investigated exhibit pronounced positive polarity dependent solvatochromic shifts of up to ~141 nm. Strong fluorescence quantum yields are also observed for dienes containing carbazole and diphenylamine donors. This behavior suggests the presence of highly polar emitting states as a result of π -π?intramolecular charge-transfer (ICT). The observations were corroborated by a linear relation of the fluorescence maximum (νmax) versus the solvent polarity function (Δf) from the Lippert-Mataga correlation. The emission lifetime shows a decay profile consistent with the formation of one species (1 and 3) and two species (2 and 4) in the excited state.

Synthesis and nonlinear optical properties of carbonylrhenium bromide complexes with conjugated pyridines

Briel, Oliver,Suenkel, Karlheinz,Krossing, Ingo,Noeth, Heinrich,Schmaelzlin, Elmar,Meerholz, Klaus,Braeuchle, Christoph,Beck, Wolfgang

, p. 483 - 490 (2007/10/03)

Carbonylrhenium bromide complexes fac-Br(OC)3ReL2 (3a,b, 4a,b) and cis-Br(OC)4ReL (5a,b) with conjugated pyridines L = Fc-CH=CH-p-C5H4N (1a), Fc-CH=CHC-(CH3)=CHCH=CHCH=C(CH3)CH=C

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