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83-24-9

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83-24-9 Usage

Synthesis Reference(s)

Journal of Medicinal Chemistry, 20, p. 1068, 1977 DOI: 10.1021/jm00218a016

Check Digit Verification of cas no

The CAS Registry Mumber 83-24-9 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 83-24:
(4*8)+(3*3)+(2*2)+(1*4)=49
49 % 10 = 9
So 83-24-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H17N/c1-10-8-9-11(2)13(10)12-6-4-3-5-7-12/h3-7,10-11H,8-9H2,1-2H3

83-24-9 Well-known Company Product Price

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  • Alfa Aesar

  • (A14614)  2,5-Dimethyl-1-phenylpyrrole, 98+%   

  • 83-24-9

  • 5g

  • 395.0CNY

  • Detail
  • Alfa Aesar

  • (A14614)  2,5-Dimethyl-1-phenylpyrrole, 98+%   

  • 83-24-9

  • 25g

  • 1517.0CNY

  • Detail

83-24-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-Dimethyl-1-phenylpyrrole

1.2 Other means of identification

Product number -
Other names 2,5-DIMETHYL-1-PHENYLPYRROLE

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:83-24-9 SDS

83-24-9Relevant articles and documents

Multimolecular self-organization of acetylene and arylamines into 1-aryl-3-ethyl-4-vinylpyrroles in the KOBut/DMSO system

Ivanova, Elena V.,Schmidt, Elena Yu.,Semenova, Nadezhda V.,Trofimov, Boris A.,Ushakov, Igor A.

, p. 315 - 317 (2020)

A new superbase-driven self-organization of four molecules of acetylene with one molecule of arylamine to 1-aryl-3ethyl-4-vinylpyrroles in the KOBut/DMSO system has been discovered. The process includes four acts of nucleophilic addition to acetylene followed by intramolecular cyclization of intermediate N,N-bis(1,3-dienyl)-N-arylamine.

A convenient approach for the synthesis of substituted pyrroles by using phosphoric acid as a catalyst and their photophysical properties

Ai, Liankun,Ibrahim, Yusuf Ajibola,Li, Baolin,Li, Jiahui

, (2021/12/21)

Twenty-three new pyrrole compounds aside from six knowns, including the synthetically challenging tetra- and penta-substituted pyrroles from the corresponding 1,4-dicarbonyl through Paal-Knorr synthesis in the presence of 5% phosphoric acid as the catalyst. Our method is noteworthy for cheap catalyst, uncomplicated experimental setup under air atmosphere, scalability, and excellent yields. The fluorescence of some selected pyrroles was investigated in dilute solution, and we found that all novel pyrroles emit strong blue fluorescences with considerable Stokes shifts.

A Highly Dispersed Copper Nanoparticles Catalyst with a Large Number of Weak Acid Centers for Efficiently Synthesizing the High Value-Added 3-Methylindole by Aniline and Biomass-Derived Glycerin

Sun, Pinghui,Lin, Shuyi,Guo, Huimei,Su, Jianhui,Shi, Lei

, p. 463 - 477 (2020/07/16)

Abstract: An excellent catalyst with a large number of weak acid centers and highly dispersed copper nanoparticles embedded in mesoporous SBA-15 carrier was successfully constructed for the purpose of efficient conversion of aniline with biomass-derived glycerin to the high value-added 3-methylindole, in which the catalyst of Cu/SBA-15 was modified with Al2O3, La2O3 and CoO in sequence. The modified carrier and the copper-based catalysts were studied by scanning electron microscopy and energy-dispersive X-ray (SEM–EDX) spectroscopy, nitrogen physical adsorption, ammonia temperature programmed desorption (NH3-TPD), hydrogen temperature programmed reduction (H2-TPR), powder X-ray diffraction (XRD), transmission electron microscopy (TEM), thermogravimetric and differential thermal analysis (TG–DTA) and inductively coupled plasma (ICP) emission spectroscopy. The research found that the Cu/CoO/La2O3/Al2O3/SBA-15 catalyst exhibited a very good catalytic performance with 3-methylindole yield up to 73.3% and selectivity reaching 86.4%. Besides, only a 3.9% yield decreased after the catalyst was circulated seven times. The characterizations revealed that Al2O3 could enhance the polarity of the carrier, thereby the interaction between the active component and the composite carrier was strengthened and the dispersion of copper was increased significantly. Adding La2O3 to Cu/SBA-15-Al2O3 could weaken the acidity and inhibit the formation of carbon deposits. CoO promoter could increase the number of weak acid centers, which was conducive to a good dispersion of active component and the high selectivity of 3-methylindole. Furthermore, the reaction pathway of gas-phase synthesis of 3-methylindole from glycerin and aniline on Cu/CoO/La2O3/Al2O3/SBA-15 was explored. Graphic Abstract: [Figure not available: see fulltext.]

Facile fabrication of porous magnetic covalent organic frameworks as robust platform for multicomponent reaction

Azizi, Najmedin,Heidarzadeh, Fatemeh,Farzaneh, Fezeh

, (2021/07/26)

The design of cheap yet efficient nanoporous magnetic catalysts for the environmentally benign process's widespread application is an extremely attractive, challenging chemical research field. A novel porous magnetic covalent organic framework was prepared by the condensation reaction of melamine and terephthaladehyde on the surface of 3,4-dihydroxybenzaldehyde coated magnetic Fe3O4 nanoparticles COF@Fe3O4 under hydrothermal conditions for the first time. The high surface area magnetic COF could exhibit superior catalytic activity for sustainable synthesis of trisubstituted and tetrasubstituted imidazoles and pyrroles in good to excellent yields in PEG as solvent under environmentally friendly, ambient conditions and making the overall process economical, efficient, and green. The retrievable catalyst in PEG is general and applicable to a broad substrate scope and functional group compatibility. The structure and morphology of the COF@Fe3O4 were characterized by FTIR, XRD, EDX, and SEM spectroscopy. The COF@Fe3O4 magnetic catalyst was recovered by an external magnet and used for several cycles without significant catalytic activity loss.

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