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3H-Indolium, 2,3,3-trimethyl-1-(phenylmethyl)-, iodide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

144723-42-2

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144723-42-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144723-42-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,7,2 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 144723-42:
(8*1)+(7*4)+(6*4)+(5*7)+(4*2)+(3*3)+(2*4)+(1*2)=122
122 % 10 = 2
So 144723-42-2 is a valid CAS Registry Number.

144723-42-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-2,3,3-trimethylindol-1-ium,iodide

1.2 Other means of identification

Product number -
Other names iodure de 1-benzyl 2,3,3-trimethylindoleninium

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:144723-42-2 SDS

144723-42-2Relevant academic research and scientific papers

Colorimetric Cyanide Chemosensor Based on 1′,3,3′,4-Tetrahydrospiro[chromene-2,2′-indole]

Dagiliene, Migle,Martynaitis, Vytas,Kri??iuˉniene, Vilija,Krik?tolaityte, Sonata,?a?kus, Algirdas

, p. 363 - 369 (2015)

A new class of chemosensors based on the 1′,3,3′,4-tetrahydrospiro[chromene-2,2′-indole] ring system, which detects cyanide with high specificity, is described. These chemosensors show a distinct color change when treated with cyanide in acetonitrile solution buffered with sodium phosphate, and this procedure is not affected by the presence of other common anions. The chemisensors exhibit high sensitivity to low concentrations of cyanide, meeting the European Union water quality control criterion of sensitivity below 0.05 mg L-1, and show a very fast response within tens of seconds. The mechanism for detection is rationalized by the nucleophilic substitution of the phenolic oxygen atom at the indoline C-2 atom by the cyanide anion to form a stable indolylnitrile adduct and to generate the colored 4-nitrophenolate chromophore. These chemosensors can be synthesized by a simple procedure from commercially available starting materials.

SYNTHESE DE QUELQUES SPIRO ET SPIRO PHOTOCHROMIQUES. APPLICATION DE LA METHODOLOGIE DE LA RECHERCHE EXPERIMENTALE

Pottier, E.,Sergent, M.,Luu, R. Phan Tan,Guglielmetti, R.

, p. 719 - 740 (2007/10/02)

Some spiro I and spiro II substituted by different groups were synthesized in order to evaluate their photochromic properties and to optimize the preparation of spiroheterocyclic systems.In addition, some spiro III were also prepared as reference compounds.Their physical and spectroscopic characteristics (UV, 1H and 13C) were determined.A study using the experimental design methodology allowed to point out the most important factors for improving the reaction yields. KEYWORDS: Photochromism, spirooxazines, spiropyrans, synthesis, 1H NMR, experimental design methodology.

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