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2,3-diphenylindolizine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21812-61-3

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21812-61-3 Usage

Chemical compound

2,3-diphenylindolizine

Molecular structure

Contains two benzene rings and a fused five-membered nitrogen-containing ring

Classification

Type of indolizine, a class of heterocyclic compounds

Potential applications

Materials science, pharmaceutical research

Studied uses

Fluorescent probe in bioimaging, building block for synthesizing novel organic molecules

Unique properties

Interesting structure and properties for further investigation and potential applications in science and technology

Check Digit Verification of cas no

The CAS Registry Mumber 21812-61-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,8,1 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 21812-61:
(7*2)+(6*1)+(5*8)+(4*1)+(3*2)+(2*6)+(1*1)=83
83 % 10 = 3
So 21812-61-3 is a valid CAS Registry Number.
InChI:InChI=1/C20H15N/c1-3-9-16(10-4-1)19-15-18-13-7-8-14-21(18)20(19)17-11-5-2-6-12-17/h1-15H

21812-61-3SDS

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-diphenylindolizine

1.2 Other means of identification

Product number -
Other names Indolizine,2,3-diphenyl

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:21812-61-3 SDS

21812-61-3Relevant academic research and scientific papers

Magnetically recoverable nickel-palladium alloy nanocatalysts for direct C-H arylation reactions

Kilic, Haydar,Lafzi, Ferruh,Metin, ?nder,Sevim, Melike,Zozik, Yunus

supporting information, p. 17515 - 17523 (2021/12/17)

Novel magnetically recoverable nanocatalyst comprising nickel-palladium (NiPd) alloy nanoparticles (NPs) supported on reduced graphene oxide (rGO) modified with cobalt ferrite (CoFe2O4) NPs was fabricated for the direct C-H arylation of imidazopyridine, imidazole, indolizine and furan with aryl halides. To prepare the presented catalyst, rGO nanosheets were first modified with as-synthesized CoFe2O4 NPs and then the obtained CoFe2O4-rGO nanocomposites served as a support material for the synthesis of bimetallic NiPd alloy NPs at various compositions. The obtained CoFe2O4-rGO/NiPd nanocatalysts were characterized by many advanced analytical techniques including TEM, STEM-EDS, XRD, XPS, and ICP-MS. Next, to optimize the reaction conditions, CoFe2O4-rGO/NiPd nanocatalysts with different alloy compositions and their monometallic counterparts (CoFe2O4-rGO/Ni and CoFe2O4-rGO/Pd) were initially tested in the direct C-H arylation of imidazopyridine with bromobenzene. Among all tested nanocatalysts under the optimum reaction conditions, CoFe2O4-rGO/Ni20Pd80 showed the best catalytic activity in terms of the isolated product yields. The C-H arylation reactions were studied over a broad substrate scope (35 examples from 36 substrates) and gave the related biaryl products in good to excellent yields. Besides a broad substrate scope, the late-stage C-H arylation of zolimidine, a gastroprotective drug, was realized under the optimized reaction conditions. Moreover, the CoFe2O4-rGO/Ni20Pd80 nanocatalysts were recovered from the reaction medium using a simple magnet and reused in the C-H arylation reactions up to five consecutive runs without a significant drop in the product yield. This study shows that magnetically recoverable Pd nanoalloys are promising heterogeneous catalysts to be used in sustainable C-H functionalization reactions.

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