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3,4-DI(FURAN-2-YL)-1-(PYRIDIN-2-YL)-5,6,7,8-TETRAHYDROISOQUINOLINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

692729-85-4

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692729-85-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 692729-85-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,2,7,2 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 692729-85:
(8*6)+(7*9)+(6*2)+(5*7)+(4*2)+(3*9)+(2*8)+(1*5)=214
214 % 10 = 4
So 692729-85-4 is a valid CAS Registry Number.

692729-85-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-bis(furan-2-yl)-1-pyridin-2-yl-5,6,7,8-tetrahydroisoquinoline

1.2 Other means of identification

Product number -
Other names 3,4-DI(FURAN-2-YL)-1-(PYRIDIN-2-YL)-5,6,7,8-TETRAHYDROISOQUINOLINE

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:692729-85-4 SDS

692729-85-4Downstream Products

692729-85-4Relevant academic research and scientific papers

Highly substituted pyridines via tethered imine-enamine (TIE) methodology

Raw, Steven A.,Taylor, Richard J. K.

, p. 508 - 509 (2004)

A tethered imine-enamine methodology has been developed for the direct conversion of 1,2,4-triazines into highly substituted pyridines via the inverse electron demand Diels-Alder reaction which avoids the need for a discrete aromatisation step. This TIE methodology has also been applied in one pot reaction cascades involving 1,2,4-triazines and utilising MnO 2-mediated tandem oxidation processes (TOPs).

Improved and practical procedures for the preparation of highly substituted pyridines and pyridazines via silica-mediated aromatisation

Catozzi, Nicola,Bromley, William J.,Wasnaire, Pierre,Gibson, Mairi,Taylor, Richard J. K.

, p. 2217 - 2221 (2008/02/10)

A new and straightforward procedure is described for the preparation of highly substituted pyridines and pyridazines. The method involves a Diels-Alder/retro-Diels-Alder sequence leading to dihydropyridine or related intermediates, which can be aromatized

Improved methodologies for the preparation of highly substituted pyridines

Sainz, Yolanda Fernandez,Raw, Steven A.,Taylor, Richard J. K.

, p. 10086 - 10095 (2007/10/03)

Two separate strategies have been developed for the preparation of highly substituted pyridines from 1,2,4-triazines via the inverse-electron-demand Diels-Alder reaction: a microwave-promoted, solvent-free procedure and a tethered imine-enamine (TIE) appr

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