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18125-24-1

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18125-24-1 Usage

General Description

Benzo[f]quinoline-3-carbonitrile is a chemical compound with the molecular formula C15H9N. It is a member of the quinoline family and contains a carbonitrile functional group. Benzo[f]quinoline-3-carbonitrile is often used as a building block in the synthesis of complex organic molecules, and it has been studied for its potential pharmaceutical applications. Benzo[f]quinoline-3-carbonitrile has been found to exhibit antimicrobial and anticancer activities in various biological assays, making it a subject of interest for drug discovery and development. Its unique structure and reactivity make it a versatile starting material for the synthesis of diverse organic compounds with potential therapeutic properties.

Check Digit Verification of cas no

The CAS Registry Mumber 18125-24-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,2 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 18125-24:
(7*1)+(6*8)+(5*1)+(4*2)+(3*5)+(2*2)+(1*4)=91
91 % 10 = 1
So 18125-24-1 is a valid CAS Registry Number.

18125-24-1SDS

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 Benzo[f]quinoline-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 2-cyano-5,6-benzoquinoline

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:18125-24-1 SDS

18125-24-1Upstream product

18125-24-1Relevant articles and documents

Iodine-catalyzed ammoxidation of methyl arenes

Guo, Songjin,Wan, Gen,Sun, Song,Jiang, Yan,Yu, Jin-Tao,Cheng, Jiang

supporting information, p. 5085 - 5088 (2015/03/30)

The development of organic transformation using cheap and readily available substrates under mild conditions will be pivotal for green and sustainable synthetic organic chemistry. Concerning our continued interest in the cyanation reaction, a metal-free direct ammoxidation of readily available methyl arenes leading to nitriles was established under mild conditions. A series of aryl methanes especially heteroaryl methanes (30 examples) were applicable in moderate to good yields with good functionality tolerance.

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