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Phenol, 2-[[3-[4-(dimethylamino)phenyl]-2-propenylidene]amino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

140913-96-8

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140913-96-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 140913-96-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,9,1 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 140913-96:
(8*1)+(7*4)+(6*0)+(5*9)+(4*1)+(3*3)+(2*9)+(1*6)=118
118 % 10 = 8
So 140913-96-8 is a valid CAS Registry Number.

140913-96-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[3-[4-(dimethylamino)phenyl]prop-2-enylideneamino]phenol

1.2 Other means of identification

Product number -
Other names 2-(4-dimethylaminocinnamalamino)phenol

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:140913-96-8 SDS

140913-96-8Relevant academic research and scientific papers

Condensation of p-dimethylaminocinnamaldehyde with aniline and substituted anilines in micellar media

Doronin,Chernova,Gusakova

, p. 261 - 267 (2005)

Optimal conditions were found for the reactions of aniline and its hydroxy-, carboxy-, methyl-, and nitro-substituted derivatives with p-dimethylaminocinnamaldehyde in the presence of sodium dodecyl sulfate micelles in the pH range 1-6. A correlation was revealed between the optimal pH value pK a of aromatic amines. The reaction in the model system aniline-p-dimethylaminocinnamaldehyde-sodium dodecyl sulfate in micelles formed by anionic surfactants is accelerated more than 1000-fold due to increased concentration of the reactive species in sodium dodecyl sulfate micelles. 2005 Pleiades Publishing, Inc.

Determination of the stability constants of the proton and Cu(II) complexes of 2-(4-dimethylaminocinnamalamino)phenol in binary solvent mixtures by the potentiometric method

Cankurtaran, Huesnue,Kunt, Goenuel,Yalcin, Mustafa

, p. 705 - 710 (2007/10/03)

The successive formation constants of copper(II) and proton complexes of the Schiff base, 2-(4-dimethylaminocinnamalamino)phenol (DACAP) formed by condensation reaction of 4-dimethylamianocinnamaldehyde and 2-aminophenol were determined in the aqueous solutions of acetone and dioxane at 25 ± 0.1°C and an ionic strength of 0.1 M by potentiometric pH measurements. Calculations were performed with the weighted least square method by means of the PKAS and BEST computer programs. The distribution diagram of the complex species was drawn as a function of the pH. The solvent effect on different protonation sites of the ligand was discussed. Some characteristic specifications of the ligand and the copper(II) complex were also described. Together with the formation of [CuL]+ and CuL2, complexes, the presence of CuL(OH)n(n-1)- hydroxo complexes were also observed at rather basic region and their corresponding formation constants were determined.

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