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4-DIBUTYLAMINOCINNAMALDEHYDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90134-11-5

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90134-11-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90134-11-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,1,3 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 90134-11:
(7*9)+(6*0)+(5*1)+(4*3)+(3*4)+(2*1)+(1*1)=95
95 % 10 = 5
So 90134-11-5 is a valid CAS Registry Number.
InChI:InChI=1/C17H25NO/c1-3-5-13-18(14-6-4-2)17-11-9-16(10-12-17)8-7-15-19/h7-12,15H,3-6,13-14H2,1-2H3

90134-11-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Dibutylaminocinnamadehyde

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:90134-11-5 SDS

90134-11-5Relevant academic research and scientific papers

Nanoscale phase analysis of molecular cooperativity and thermal transitions in dendritic nonlinear optical glasses

Knorr, Daniel B.,Benight, Stephanie J.,Krajina, Brad,Zhang, Cheng,Dalton, Larry R.,Overney, René M.

, p. 13793 - 13805 (2013/01/16)

A broad nanoscopic study of a wide-range of dendritic organic nonlinear optical (NLO) self-assembly molecular glasses reveals an intermediate thermal phase regime responsible for both enhanced electric field poling properties and strong phase stabilizatio

NONLINEAR OPTICAL COMPOUNDS AND METHODS FOR THEIR PREPARATION

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Page 32; 14/19, (2010/02/07)

Nonlinear optically active compounds, methods for making nonlinear optically active compounds, compounds useful for making nonlinear optically active compounds, methods for making compounds useful for making nonlinear optically active compounds, macrostructures tha tinclude nonlinear optically active components, and devices including the nonlinear optically active compounds and the macrostructures.

Amphiphilic polyenic push-pull chromophores for nonlinear optical applications

Alain, Valerie,Blanchard-Desce, Mireille,Ledoux-Rak, Isabelle,Zyss, Joseph

, p. 353 - 354 (2007/10/03)

Amphiphilic cationic polyenic push-pull chromophores which offer interesting supramolecular possibilities for second harmonic generation have been synthesised and their optical non-linearities studied for the first time by electric field induced second ha

Intramolecular electron density redistribution upon hydrogen bond formation in the anion Methyl Orange at the water/1,2-dichloroethane interface probed by phase interference second harmonic generation

Rinuy, Juliette,Piron, Alexis,Brevet, Pierre Francois,Blanchard-Desce, Mireille,Girault, Hubert H.

, p. 3434 - 3441 (2007/10/03)

Surface second harmonic generation (SSHG) studies of the azobenzene derivative p-dimethylaminoazobenzene sulfonate, often referred as Methyl Orange (MO), at the neat water/1,2-dichloroethane (DCE) interface is reported. The two forms of the anionic MO dye

Large quadratic hyperpolarizabilities with donor-acceptor polyenes exhibiting optimum bond length alternation: Correlation between structure and hyperpolarizability

Blanchard-Desce,Alain,Bedworth,Marder,Fort,Runser,Barzoukas,Lebus,Wortmann

, p. 1091 - 1104 (2007/10/03)

Donor acceptor polyenes of various lengths, and that combine aromatic electron-donating moieties with powerful heterocyclic electron-withdrawing terminal groups, have been synthesized and characterized as efficient nonlinear optical (NLO) chromophores. Th

Charge-Shift Probes of Membrane Potential. Synthesis

Hassner, A.,Birnbaum, D.,Loew, L. M.

, p. 2546 - 2551 (2007/10/02)

We are reporting two general synthetic approaches to a number of (aminostyryl)pyridinium dyes and their heterocyclic analogues which are of interest as electrochromic probes for membrane potential.The two routes which involve palladium-catalyzed coupling or aldol condensation permit considerable structure variations to be introduced in the dyes.Some spectral properties of the dyes are discussed.

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