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2-Naphthalenamine, N-[(2-chlorophenyl)methylene]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27587-15-1

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27587-15-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27587-15-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,5,8 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 27587-15:
(7*2)+(6*7)+(5*5)+(4*8)+(3*7)+(2*1)+(1*5)=141
141 % 10 = 1
So 27587-15-1 is a valid CAS Registry Number.

27587-15-1Relevant academic research and scientific papers

A stereoselective Povarov reaction leading to exo-tetrahydroindolo[3,2-c] quinoline derivatives catalyzed by iodine

Wang, Xiang-Shan,Yin, Ming-Yue,Wang, Wei,Tu, Shu-Jiang

experimental part, p. 4811 - 4818 (2012/09/22)

We report an iodine-catalyzed Povarov reaction using indole as dienophile carried out in toluene at room temperature. This three-component reaction, coupling an aldehyde, an amine, and an indole, proved to be an efficient method for synthesizing exo-indol

An efficient method for the synthesis of benzo[f]quinoline and benzo[a]phenanthridine derivatives catalyzed by iodine by a three-component reaction of arenecarbaldehyde, naphthalen-2-amine, and cyclic ketone

Wang, Xiang-Shan,Li, Qing,Yao, Chang-Sheng,Tu, Shu-Jiang

body text, p. 3513 - 3518 (2009/04/07)

A mild, efficient, and general method for the synthesis of benzo[f]quinoline and benzo[a]phenanthridine derivatives by a three-component reaction of arenecarbaldehyde, naphthalen-2-amine, and cyclic ketone using iodine as catalyst is described. A possible

Reaction of β-Arylidennaphthylamines with 4-Hydroxycoumarin. A Correction in Structural Assignment of the Product. III.

Martinez, Roberto,Cortes, Eduardo,Toscano, Ruben A.,Alfaro, L. Josue

, p. 1273 - 1276 (2007/10/02)

The reaction of 4-hydroxycoumarin with β-arylidennaphthylamines constitutes a convenient synthetic route to the hitherto unknown 2H-benzobenzopyranoquinolin-2-one, VI.The X-ray crystallography data conform with the present benzopyranoq

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