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3-butyl-4-pentylquinolin-2(1H)-one is a complex organic compound belonging to the quinolinone family, characterized by a quinoline ring system with a 2(1H)-one functional group. 3-butyl-4-pentylquinolin-2(1H)-one features a butyl group attached to the 3-position and a pentyl group at the 4-position of the quinoline nucleus. The presence of these alkyl chains contributes to its lipophilic nature, which may influence its solubility and potential biological activity. The compound's structure and properties make it a subject of interest in chemical research, particularly in the fields of medicinal chemistry and material science, where it could be explored for various applications, such as in the development of new drugs or as a component in advanced materials.

6017-89-6

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6017-89-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6017-89-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,1 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6017-89:
(6*6)+(5*0)+(4*1)+(3*7)+(2*8)+(1*9)=86
86 % 10 = 6
So 6017-89-6 is a valid CAS Registry Number.

6017-89-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Butyl-4-oxo-3,4,5,6,7,8-hexahydro-1,2,3-benzotriazin

1.2 Other means of identification

Product number -
Other names 3-butyl-5,6,7,8-tetrahydro-3H-benzo[d][1,2,3]triazin-4-one

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:6017-89-6 SDS

6017-89-6Downstream Products

6017-89-6Relevant academic research and scientific papers

Palladium-catalyzed intermolecular domino reaction of gem-dibromoenynes with anilines; A one-pot synthesis of quinolines and quinolinones

Meng, Tianhao,Zhang, Wen-Xiong,Zhang, Hui-Jun,Liang, Yun,Xi, Zhenfeng

, p. 2754 - 2762 (2012/11/07)

An efficient domino process involving palladium-catalyzed amination of an alkenyl bromide, 1,5-H transfer, annulation via 6-exo-dig electrophilic cyclization, and palladium-catalyzed etherification, is described. This reaction provides an efficient one-pot synthesis of multi-substituted quinolines and quinolinones from gem-dibromoenynes and anilines. Georg Thieme Verlag Stuttgart New York.

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