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2-Naphthalenamine, N-[(4-bromophenyl)methylene]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53600-19-4

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53600-19-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53600-19-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,0 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53600-19:
(7*5)+(6*3)+(5*6)+(4*0)+(3*0)+(2*1)+(1*9)=94
94 % 10 = 4
So 53600-19-4 is a valid CAS Registry Number.

53600-19-4SDS

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 1-(4-bromophenyl)-N-naphthalen-2-ylmethanimine

1.2 Other means of identification

Product number -
Other names N-[(4-bromophenyl)methylene]-2-naphthalenamine

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:53600-19-4 SDS

53600-19-4Relevant academic research and scientific papers

An efficient method for the synthesis of indolo[3,2-c]quinoline derivatives catalyzed by iodine

Zhou, Yujing,Zhang, Meimei,Yin, Mingyue,Wang, Xiangshan

, p. 237 - 242 (2013)

The reaction of Schiff base and indole catalyzed by iodine in DMA, subsequently treated with DDQ, gave indolo[3,2-c]quinoline derivatives in good yields. The structure of 3e was confirmed by X-ray diffraction analysis. The reaction of Schiff base and indo

Synthesis of 5-aryl-1,2,3,4-tetrahydrobenzo[a]phenanthridines

Kozlov,Basalaeva

, p. 250 - 256 (2007/10/03)

Previously unknown derivatives of tetrahydro[a]phenanthridine containing annelated benzoquinoline and cyclohexene nuclei were prepared by condensation of azomethines of the 2-naphthylamine series with cyclohexanone. The possibility of synthesis of such compounds without preliminarily preparing Schiff bases was demonstrated. The effect of substituents in the aromatic ring of the azomethine on the yield of the target products was elucidated. The IR, UV, 1H NMR, and mass spectra of the synthesized compounds were discussed.

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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