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6-Chloroquinolin-5-amine is a chemical compound that belongs to the quinoline family. It is characterized by its chloro and amino functional groups, which are located at the 6 and 5 positions of the quinoline ring structure, respectively. 6-CHLOROQUINOLIN-5-AMINE is primarily used as a chemical intermediate or building block for the synthesis of various other compounds due to its versatile reactivity. Although it has inherent bioactivity associated with quinolines, its specific applications largely depend on the compounds derived from it. However, detailed information about its toxicity and environmental impact is not readily available, and further research may be necessary for a comprehensive understanding of its properties.

341010-40-0

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341010-40-0 Usage

Uses

Used in Pharmaceutical Industry:
6-Chloroquinolin-5-amine is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its chloro and amino functional groups provide a versatile platform for the development of new drugs with potential therapeutic applications.
Used in Chemical Research:
6-Chloroquinolin-5-amine is used as a building block in chemical research to explore its reactivity and potential for forming new compounds. This can lead to the discovery of novel chemical entities with unique properties and applications.
Used in Material Science:
6-Chloroquinolin-5-amine may be used as a component in the development of new materials, such as organic electronic devices or advanced materials with specific properties. Its reactivity and functional groups can contribute to the creation of innovative materials with improved performance.
Note: The specific applications mentioned above are hypothetical and based on the general properties of 6-chloroquinolin-5-amine. Further research and development would be required to validate these uses and explore additional potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 341010-40-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,1,0,1 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 341010-40:
(8*3)+(7*4)+(6*1)+(5*0)+(4*1)+(3*0)+(2*4)+(1*0)=70
70 % 10 = 0
So 341010-40-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H7ClN2/c10-7-3-4-8-6(9(7)11)2-1-5-12-8/h1-5H,11H2

341010-40-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-CHLOROQUINOLIN-5-AMINE

1.2 Other means of identification

Product number -
Other names 5-Amino-6-chloroquinoline

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:341010-40-0 SDS

341010-40-0Downstream Products

341010-40-0Relevant articles and documents

Efficient and recyclable bimetallic Co–Cu catalysts for selective hydrogenation of halogenated nitroarenes

Lu, Xionggang,Ren, Jiaan,Sheng, Yao,Wang, Xueguang,Wu, Baoqin,Zou, Xiujing

, (2021/12/20)

Silica supported N-doped carbon layers encapsulating Co–Cu nanoparticles (Co1Cux@CN/SiO2) were prepared by a one-step impregnation of Co(NO3)2·6H2O, Cu(NO3)2·3H2O, urea and glucose, following in situ carbothermal reduction. Effects of Cu contents on the catalytic performance of the Co1Cux@CN/SiO2 catalysts were investigated for selective hydrogenation of p-chloronitrobenzene to p-chloroaniline. The Co1Cu0.30@CN/SiO2 with Cu/Co molar ratio of 0.30:1 presented much higher activity and stability than the monometallic Co@CN/SiO2 catalyst. The addition of Cu into Co1Cux@CN/SiO2 catalysts had favorable effects on the formation of highly active Co–N sites and N-doped carbon layer. The role of the N-doped carbon layer was to protect the Co from oxidation by air, and the Co1Cu0.30@CN/SiO2 could be reused for at least 12 cycles without decrease in catalytic efficiency. Mechanistic and in situ infrared studies revealed that the interaction effect between the Co and Cu atoms made the surface of Co highly electron rich, which decreased adsorption of halogen groups and resulting in the enhanced selectivity during chemoselective hydrogenation of halogenated nitroarenes for a wide scope of substrates.

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