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21255-17-4

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21255-17-4 Usage

General Description

2-Phenyl-7-Methoxyquinoline, also known as 7-methoxy-2-phenylquinoline, is a chemical compound with the molecular formula C17H13NO. It is an aromatic organic compound with a quinoline backbone and a phenyl and methoxy substituent. 2-Phenyl-7-Methoxyquinoline has potential medicinal properties, as it has been studied for its potential applications in the treatment of cancer and other diseases. Its structure and properties make it a candidate for drug development and further research in the field of medicinal chemistry. Additionally, it has been investigated for its fluorescent properties and potential applications in materials science and organic electronics.

Check Digit Verification of cas no

The CAS Registry Mumber 21255-17-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,2,5 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 21255-17:
(7*2)+(6*1)+(5*2)+(4*5)+(3*5)+(2*1)+(1*7)=74
74 % 10 = 4
So 21255-17-4 is a valid CAS Registry Number.

21255-17-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-Methoxy-2-phenylquinoline

1.2 Other means of identification

Product number -
Other names 2-Phenyl-7-methoxyquinoline

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:21255-17-4 SDS

21255-17-4Relevant articles and documents

Heteroannulation of 3-Bis(methylthio)acrolein with Aromatic Amines - A Convenient Highly Regioselective Synthesis of 2-(Methylthio)quinolines and their Benzo/Hetero Fused Analogs: A Modified Skraup Quinoline Synthesis

Panda, Kausik,Siddiqui, Iffat,Mahata, Pranab K.,Ila, Hiriyakkanavar,Junjappa, Hiriyakkanavar

, p. 449 - 452 (2004)

A simple and efficient synthesis of 2-(methylthio)quinolines and their condensed analogs has been developed through acid-induced cyclocondensation of their respective anilines or aromatic diamines with 3-bis(methylthio)acrolein. The 2-(methylthio) functionality in these quinolines could be either dethiomethylated or replaced by various nitrogen and carbon nucleophiles to afford 2-substituted quinolines.

Preparation of 2-Arylquinolines from 2-Arylethyl Bromides and Aromatic Nitriles with Magnesium and N -Iodosuccinimide

Naruto, Hiroki,Togo, Hideo

, p. 1122 - 1130 (2020/04/01)

Treatment of 2-arylethylmagnesium bromides, prepared from 2-arylethyl bromides and magnesium, with aromatic nitriles, followed by reaction with water and then with N -iodosuccinimide under irradiation with a tungsten lamp, gave the corresponding 2-arylquinolines in good to moderate yields under transition-metal-free conditions. 2-Alkylquinolines could be also obtained in moderate yields by the same procedure with 2-arylethyl bromides, magnesium, aliphatic nitriles bearing a secondary alkyl group, and N -iodosuccinimide.

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