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1H-Indole-2-carboxamide,N-methyl-Nphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62048-32-2

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62048-32-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62048-32-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,0,4 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 62048-32:
(7*6)+(6*2)+(5*0)+(4*4)+(3*8)+(2*3)+(1*2)=102
102 % 10 = 2
So 62048-32-2 is a valid CAS Registry Number.

62048-32-2SDS

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 N-methyl-N-phenyl-1H-indole-2-carboxamide

1.2 Other means of identification

Product number -
Other names N-methyl-N-phenylindole-2-carboxamide

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:62048-32-2 SDS

62048-32-2Relevant academic research and scientific papers

Synthesis of Indolo[2,3- c]quinolin-6(7 H)-ones and Antimalarial Isoneocryptolepine. Computational Study on the Pd-Catalyzed Intramolecular C-H Arylation

Szabó, Tímea,Papp, Marcell,Németh, Dóra Rita,Dancsó, András,Volk, Balázs,Milen, Mátyás

supporting information, p. 128 - 145 (2020/12/22)

The synthesis of variously substituted indolo[2,3-c]quinolin-6(7H)-ones was developed via Pd-catalyzed intramolecular C-H arylation. This method highlights a strategy for preparing indoloquinoline precursors bearing versatile functional groups and provide

One-pot synthesis of indolo[2,3-c]quinolin-6-ones by sequential photocyclizations of 3-(2-azidophenyl)-N-phenylacrylamides

Li, Zhanshan,Wang, Weixia,Zhang, Xiaotian,Hu, Congcong,Zhang, Wei

, p. 73 - 78 (2013/04/24)

A one-pot synthesis of indolo[2,3-c]quinolin-6(7H)-ones was achieved by sequential photocyclizations of 3-(2-azidophenyl)-N-phenylacrylamides in moderate to high yields. The reactions proceeded via photochemical cyclization of aryl azides to form N-phenylindol-2-carbamides and subsequent 6π-electrocyclic reaction and oxidative aromatization to afford the corresponding indolo[2,3-c]quinolin-6(7H)-ones. Georg Thieme Verlag Stuttgart · New York.

Preparation of indole-2-carboxamides by palladium-catalyzed carbonylation

Herbert, John M.,McNeill, Alan H.

, p. 2421 - 2424 (2007/10/03)

Palladium-mediated carbonylation of a 2-iodoindole in the presence of an amine provides an efficient method for the preparation of indole-2- carboxamides. The process is clean and rapid, and appears to be general where the amine component is sufficiently nonvolatile.

Functionalisation of the Alkoxy Group of Alkyl Aryl Ethers. Demethylation, Alkylthiolation and Reduction of 5-Methoxyindoles

Caubere, Catherine,Caubere, Paul,Renard, Pierre,Bizot-Espiart, Jean-Guy,Ianelli, Sandra,et al.

, p. 13433 - 13448 (2007/10/02)

In the presence of AlX3-RSH three kinds of reactions may take place with 5-methoxy indoles: demethylation, alkylthiolation and reduction.The two latter reactions have never been observed to the present, with such reagents.Considerable improvement in the s

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