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Pyridine, 2-(3,5-diphenyl-1H-pyrazol-1-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76211-98-8

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76211-98-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76211-98-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,2,1 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 76211-98:
(7*7)+(6*6)+(5*2)+(4*1)+(3*1)+(2*9)+(1*8)=128
128 % 10 = 8
So 76211-98-8 is a valid CAS Registry Number.

76211-98-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3,5-diphenylpyrazol-1-yl)pyridine

1.2 Other means of identification

Product number -
Other names -

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:76211-98-8 SDS

76211-98-8Relevant academic research and scientific papers

AIEE phenomenon: Tetraaryl vs. triaryl pyrazoles

Mukherjee, Sayani,Salini,Srinivasan,Peruncheralathan

supporting information, p. 17148 - 17151 (2015/12/05)

Tetraarylpyrazoles are synthesized from commercially available materials in three steps and found to exhibit Aggregation Induced Emission Enhancement (AIEE) characteristics. Removing one aryl unit from tetraarylpyrazole leads to Aggregation Caused Quenching (ACQ), thus the number of aryl groups plays an important role in exploring such a phenomenon.

Synthesis of tri- and tetrasubstituted pyrazoles via Ru(II) catalysis: Intramolecular aerobic oxidative C-N coupling

Hu, Jiantao,Chen, Shi,Sun, Yonghui,Yang, Jing,Rao, Yu

supporting information, p. 5030 - 5033,4 (2012/12/12)

An unprecedented ruthenium(II)-catalyzed intramolecular oxidative C-N coupling method has been developed for the facile synthesis of a variety of synthetically challenging tri- and tetrasubstituted pyrazoles. Dioxygen gas is employed as the oxidant in this transformation. The reaction demonstrates excellent reactivity, functional group tolerance, and high yields.

Regiospecific synthesis of pyrazoles from 1-azabutadiene derivatives.

a Jose,Gotor, Vicente

, p. 1478 - 1492 (2007/10/02)

Reaction of 4-amino-1-azabutadienes with different hydrazines leads to pyrazoles.On the other hand, when 4-alkylidene-1-hydrazino-1-azabutadiene derivatives are treated with trifluoroacetic acid, N-alkenylpyrazoles are obtained.

Synthesis of Heterocyclic Compounds IV Pyrazol-1'-ylpyridines

Khan, Misbahul A.,Pinto, Alvaro A. A.

, p. 883 - 888 (2007/10/02)

2-Pyrazol-1'-ylpyridines were synthesized by condensation of pyridylhydrazines with 1,3-dicarbonyl compounds or by the Ullmann arylation of pyrazoles with halopyridines. - Keywords: Arylations; Pyrazolylpyridines; Ullmann reaction

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