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871798-96-8

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871798-96-8 Usage

General Description

4-PROPYL-[2,2']BIPYRIDINYL is a chemical compound with the molecular formula C15H15N3. It is a derivative of bipyridine, consisting of two pyridine rings connected by a propyl group at the 4-position. 4-PROPYL-[2,2']BIPYRIDINYL is often used in coordination chemistry as a ligand in the synthesis of metal complexes. It has also been studied for its potential use in organic light-emitting diodes (OLEDs) and as a component in dye-sensitized solar cells. Additionally, 4-PROPYL-[2,2']BIPYRIDINYL has been investigated for its biological activities, including its potential as an anticancer agent.

Check Digit Verification of cas no

The CAS Registry Mumber 871798-96-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,7,9 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 871798-96:
(8*8)+(7*7)+(6*1)+(5*7)+(4*9)+(3*8)+(2*9)+(1*6)=238
238 % 10 = 8
So 871798-96-8 is a valid CAS Registry Number.

871798-96-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-propyl-2-pyridin-2-ylpyridine

1.2 Other means of identification

Product number -
Other names 2,2'-Bipyridine,4-propyl

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:871798-96-8 SDS

871798-96-8Downstream Products

871798-96-8Relevant articles and documents

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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