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N-ethyl-N-(3-phenylprop-2-yn-1-yl)aniline is an organic compound with the chemical formula C17H16N2. It is a derivative of aniline, featuring an ethyl group (-CH2CH3) and a 3-phenylprop-2-yn-1-yl group attached to the nitrogen atom. The 3-phenylprop-2-yn-1-yl group consists of a phenyl ring (C6H5) attached to a propargyl group (C≡CH), which is a three-carbon chain with a triple bond at one end. N-ethyl-N-(3-phenylprop-2-yn-1-yl)aniline is characterized by its aromatic nature due to the presence of the phenyl ring and the conjugated triple bond, which can participate in various chemical reactions. It is used in the synthesis of dyes, pharmaceuticals, and other organic compounds due to its unique structure and reactivity.

6279-95-4

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6279-95-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6279-95-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6279-95:
(6*6)+(5*2)+(4*7)+(3*9)+(2*9)+(1*5)=124
124 % 10 = 4
So 6279-95-4 is a valid CAS Registry Number.

6279-95-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-ethyl-N-(3-phenylprop-2-ynyl)aniline

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

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More Details:6279-95-4 SDS

6279-95-4Downstream Products

6279-95-4Relevant academic research and scientific papers

Copper-Catalyzed Tandem Sulfuration/Annulation of Propargylamines with Sulfur via C-N Bond Cleavage

Xu, Hong-Hui,Zhang, Xiao-Hong,Zhang, Xing-Guo

, p. 7894 - 7900 (2019/06/27)

Copper-catalyzed aerobic oxidative sulfuration and annulation of propargylamines with elemental sulfur is described. The tandem reaction involves C-N bond cleavage and the formation of multiple C-S bonds, affording 1,2-dithiole-3-thiones in good to excellent yields with good functional group tolerance.

Copper Photoredox Catalyzed A3’ Coupling of Arylamines, Terminal Alkynes, and Alcohols through a Hydrogen Atom Transfer Process

Sagadevan, Arunachalam,Pampana, V. Kishore Kumar,Hwang, Kuo Chu

supporting information, p. 3838 - 3842 (2019/02/26)

The first successful example of the three-component coupling of N-alkylanilines, terminal alkynes, and alcohols was achieved at room temperature by a visible-light-mediated copper-catalyzed photoredox hydrogen-atom transfer process. This method allows pre

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