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4-(P-DIMETHYLAMINOPHENYL)-2,6-DIPHENYLPYRYLIUM PERCHLORATE is a complex organic compound with the chemical formula C26H22ClNO2+. It is a derivative of pyrylium, a heterocyclic aromatic compound, and features a p-dimethylaminophenyl group attached to the 4-position of the pyrylium ring. 4-(P-DIMETHYLAMINOPHENYL)-2,6-DIPHENYLPYRYLIUM PERCHLORATE is characterized by its deep color and is often used as a dye or pigment in various applications. The perchlorate anion (ClO4-) is associated with the cationic pyrylium structure, contributing to its overall charge balance. Due to its unique structure and properties, 4-(P-DIMETHYLAMINOPHENYL)-2,6-DIPHENYLPYRYLIUM PERCHLORATE is of interest in the fields of organic chemistry and materials science, particularly for its potential use in the development of new dyes, pigments, and other specialty chemicals.

2970-29-8

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2970-29-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2970-29-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,7 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2970-29:
(6*2)+(5*9)+(4*7)+(3*0)+(2*2)+(1*9)=98
98 % 10 = 8
So 2970-29-8 is a valid CAS Registry Number.
InChI:InChI=1/C25H22NO.ClHO4/c1-26(2)23-15-13-19(14-16-23)22-17-24(20-9-5-3-6-10-20)27-25(18-22)21-11-7-4-8-12-21;2-1(3,4)5/h3-18H,1-2H3;(H,2,3,4,5)/q+1;/p-1

2970-29-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(P-DIMETHYLAMINOPHENYL)-2,6-DIPHENYLPYRYLIUM PERCHLORATE

1.2 Other means of identification

Product number -
Other names 4-<4-(dimethylamino)phenyl>-2,6-diphenylpyrylium perchlorate

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:2970-29-8 SDS

2970-29-8Relevant academic research and scientific papers

Multi-channel receptors based on thiopyrylium functionalised with macrocyclic receptors for the recognition of transition metal cations and anions

Abalos,Jimenez,Moragues,Royo,Martinez-Manez,Sancenon,Soto,Costero,Parra,Gil

, p. 3449 - 3459 (2010)

We report herein the synthesis and characterization of a family of ligands containing different cation binding sites covalently connected to a thiopyrylium signalling reporter. The receptors L1-L6 are able to signal the presence of c

Facile and Stereospecific Synthesis of Various Dienones Using Task-specific Ionic Liquid/Borohydride as Stable and Promoted Hydrogen Release Reagent

Mouradzadegun, Arash,Ganjali, Mohammad Reza,Sabbagh, Elham,Abadast, Fatemeh

, p. 3574 - 3577 (2017/11/21)

In this work, for the first time, task-specific ionic liquid, 1-n-butyl-3-methylimidazolium borohydride ([bmim]BH4), was used as the medium as well as reagent for the regiospecific reduction of triarylpyrylium perchlorates to provide aromatic d

Expeditious synthesis of aromatic cyanodienones using neutral alumina as a versatile heterogeneous catalyst

Mouradzadegun, Arash,Abadast, Fatemeh

, p. 640 - 647 (2014/01/17)

The work described herein employs neutral alumina as an effective catalyst for ring opening of triarylpyrylium perchlorates to corresponding aromatic cyanodienones, which have main roles in biological activities. The present porous catalyst has several ad

Surfactant-assisted chromogenic sensing of cyanide in water

Abalos, Tatiana,Royo, Santiago,Martinez-Manez, Ramon,Sancenon, Felix,Soto, Juan,Costero, Ana M.,Gil, Salvador,Parra, Margarita

experimental part, p. 1641 - 1645 (2009/12/23)

Chromogenic cyanide recognition in water was achieved by the use of a hydrophobic dye in micellar containers.

Process for detecting target nucleic acid, process for quantifying the same, and pyrylium compound for chemiluminescence analysis

-

, (2008/06/13)

The present invention provides a process for detecting or quantifying a target nucleic acid in a sample, the process comprising the steps of associating a chemiluminescent compound, capable of being associated with a double-stranded nucleic acid, with a double-stranded nucleic acid including the target nucleic acid, and detecting or measuring chemiluminescence derived from the chemiluminescent compound associated with the double-stranded nucleic acid. According to the process, the target nucleic acid in the sample can be highly sensitively detected, or precisely quantified.

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