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1,1,3,3-TetraMethyl-5-phenylisoindoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86762-52-9

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86762-52-9 Usage

Class

Isoindolines

Physical State

Yellow crystalline solid

Usage

Commonly used in the synthesis of organic compounds

Properties

Fluorescent

Applications

Development of fluorescent dyes and pigments

Potential Applications

Materials science, organic light-emitting diodes (OLEDs), and organic photovoltaic (OPV) devices

Safety Measures

Proper handling and use due to potential health hazards

Check Digit Verification of cas no

The CAS Registry Mumber 86762-52-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,7,6 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 86762-52:
(7*8)+(6*6)+(5*7)+(4*6)+(3*2)+(2*5)+(1*2)=169
169 % 10 = 9
So 86762-52-9 is a valid CAS Registry Number.

86762-52-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,3,3-tetramethyl-5-phenyl-2H-isoindole

1.2 Other means of identification

Product number -
Other names 1H-Isoindole,2,3-dihydro-1,1,3,3-tetramethyl-5-phenyl

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:86762-52-9 SDS

86762-52-9Downstream Products

86762-52-9Relevant academic research and scientific papers

SELECTIVITY CONTROL IN COBALT(0)-CATALYZED CYCLOADDITION REACTIONS

Chiusoli, Gian Paolo,Costa, Mirco,Zhou, Zhiming

, p. 441 - 449 (2007/10/02)

The chemistry of cobalt(0)-catalyzed cycloadditions, involving reaction of alkynes with other alkynes or with nitriles or with activated olefins is compared to that of cobalt(I).While the presence of a ?-ligand in cobalt(I) complexes controls the access t

Double Ring Closure of Diacetylenic Compounds with Activated Olefins in the Presence of a Cobalt(0) Catalyst

Zhou, Zhiming,Costa, Mirco,Chiusoli, Gian Paolo

, p. 1399 - 1406 (2007/10/02)

Ring formation from 1,6- or 1,7-diynes and activated olefins is catalysed by cobalt(0) complexes through cobaltacyclopentadiene intermediates.If steric hindrance is sufficiently low the reaction proceeds further and products containing two molecules of olefin per molecule of diyne are obtained.With terminally alkyl-substituted and conformationally rigid diynes the reaction must be carried out stoichiometrically because of the incursion of a new acid/ base-catalysed reaction, which is independent of cobalt.

PALLADIUM-CATALYZED CARBONYLATION OF ALKANES. IV. TRAPPING OF CYCLOPENTADIENONES BY DIENOPHILES

Chiusoli, Gian Paolo,Costa, Mirco,Reverberi, Sara,Salerno, Giuseppe,Terenghi, Maria Giuliana

, p. 695 - 700 (2007/10/02)

1,6-Diynes and, to a lower extent, 1,7-diynes form cyclopentadienones by means of Pd(0) catalysts under mild conditions.Dimerization of cyclopentadienones can be prevented by carrying out the reaction in the presence of suitable dienophiles which are able

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