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5469-13-6

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5469-13-6 Usage

Type of compound

Quaternary ammonium salt

Structural features

a. Quinolinium ring
b. Phenylethyl group attached to the quinolinium ring

Biological activities

a. Antibacterial properties
b. Antifungal properties

Potential applications

a. Fluorescent probe for sensing and imaging applications
b. Medicine
c. Materials science
d. Chemical biology

Versatility

The structure and properties of 1-(2-phenylethyl)quinolinium make it a potentially versatile compound with a range of potential applications in various fields.

Further research

Ongoing research and development of this compound may reveal even more promising uses and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 5469-13-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5469-13:
(6*5)+(5*4)+(4*6)+(3*9)+(2*1)+(1*3)=106
106 % 10 = 6
So 5469-13-6 is a valid CAS Registry Number.

5469-13-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-phenylethyl)quinolin-1-ium,bromide

1.2 Other means of identification

Product number -
Other names 1-Phenaethyl-chinolinium,Bromid

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:5469-13-6 SDS

5469-13-6Relevant articles and documents

Selective construction of fused heterocycles by an iridium-catalyzed reductive three-component annulation reaction

Gong, Lingzhen,Jiang, Huanfeng,Yang, Jian,Zhang, Min,Zhao, He

supporting information, p. 8292 - 8295 (2021/08/25)

Catalytic conversion of ubiquitously distributed but less reactive N-heteroarenes into functional products remains to date a challenge. Here, through an initial pretreatment of N-heteroarenes with alkyl bromide, we describe a syn-selective construction of functional fused heterocycles via iridium catalyzed reductive annulation of N-heteroarenium salts with formaldehyde and cyclic 1,3-diketones or 4-hydroxycoumarins, proceeding with broad substrate scope, good functional group compatibility, readily available feedstocks, and high step and atom efficiency.

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