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N-(naphthalen-2-yl)-4-phenylthiazol-2-amine is a complex organic compound with the molecular formula C23H17N3S. It is characterized by a thiazol-2-amine core, which is fused to a naphthalene ring at the 2-position and substituted with a phenyl group at the 4-position. N-(naphthalen-2-yl)-4-phenylthiazol-2-amine is known for its potential applications in the field of pharmaceuticals and materials science, particularly as a building block for the synthesis of various biologically active molecules and as a component in the development of new materials with specific optical or electronic properties. Its chemical structure endows it with unique physical and chemical properties, making it a subject of interest for researchers in organic chemistry and related disciplines.

1843-14-7

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1843-14-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1843-14-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,4 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1843-14:
(6*1)+(5*8)+(4*4)+(3*3)+(2*1)+(1*4)=77
77 % 10 = 7
So 1843-14-7 is a valid CAS Registry Number.

1843-14-7Downstream Products

1843-14-7Relevant academic research and scientific papers

Eco-friendly synthesis of 2-aminothiazoles using Nafion-H as a recyclable catalyst in PEG-water solvent system

Kidwai, Mazaahir,Chauhan, Ritika,Bhatnagar, Divya

, p. 37 - 44 (2011)

A simple, efficient, single step and environmentally benign synthesis of 2-aminothiazoles is described in this paper. This green protocol was catalyzed by recyclable solid supported Nafion-H using polyethylene glycol-water solvent system with improved efficiency and reduced waste production.

Facile one-pot procedure for the synthesis of 2-aminothiazole derivatives

Yin, Guodong,Ma, Junrui,Shi, Houqiang,Tao, Qing

experimental part, p. 1941 - 1948 (2012/09/07)

A facile, efficient synthesis of 2-aminothiazole derivatives by the reaction of easily available aromatic methyl ketones with thiourea/N-substituted thioureas in the presence of copper(II) bromide was developed. The reaction underwent a one-pot ?-bromination/cyclization process.

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