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14061-24-6

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14061-24-6 Usage

General Description

1,6-dimethylquinolinium is a chemical compound that belongs to the quinolinium class of chemicals. It is a quaternary ammonium salt with a molecular formula of C11H15N and a molecular weight of 161.24 g/mol. Its chemical structure consists of a quinoline ring with two methyl groups attached at the 1 and 6 positions, and a positively charged quaternary nitrogen atom. 1,6-dimethylquinolinium is often used as a reactant or catalyst in organic synthesis, particularly in the formation of various heterocyclic compounds. It has also been investigated for its potential biological activities, such as antimicrobial and anticancer properties. Its unique chemical structure and properties make it a valuable tool in synthetic and medicinal chemistry research.

Check Digit Verification of cas no

The CAS Registry Mumber 14061-24-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,6 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14061-24:
(7*1)+(6*4)+(5*0)+(4*6)+(3*1)+(2*2)+(1*4)=66
66 % 10 = 6
So 14061-24-6 is a valid CAS Registry Number.

14061-24-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,6-dimethylquinaldinium iodide

1.2 Other means of identification

Product number -
Other names 1,2,6-trimethylquinolinium iodide

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:14061-24-6 SDS

14061-24-6Relevant articles and documents

Synthesis of novel tetra- and pentacyclic benzosultam scaffolds via domino Knoevenagel hetero-Diels-Alder reactions in water

Ghandi, Mehdi,Sheibani, Shahab,Sadeghzadeh, Masoud,Daha, Fariba Johari,Kubicki, MacIej

, p. 1057 - 1065 (2013)

An efficient catalyst-free and diastereoselective synthesis of novel dihydropyrano[2,3-d]pyrimidine and dihydropyrano[3,2-c]chromen-annulated benzosultams is described. A number of (E)-N-(2-formylphenyl)-N-methyl-2- phenylethenesulfonamides were synthesized and underwent a one-pot domino Knoevenagel hetero-Diels-Alder reaction, respectively, with N,N- dimethylbarbituric acid and 4-hydroxycoumarin in water, giving the desired products, in moderate to excellent yields.

Design, Synthesis, and Antifungal Evaluation of Neocryptolepine Derivatives against Phytopathogenic Fungi

Gao, Jian-Mei,Lawoe, Raymond Kobla,Liu, Ying-Qian,Shang, Xiao-Fei,Sun, Yu,Yang, Cheng-Jie,Yin, Xiao-Dan,Zhao, Zhong-Min,Zhou, Rui,Zhu, Jia-Kai

, p. 2306 - 2315 (2020/03/10)

Neocryptolepine is an alkaloid isolated from traditional African herbal medicine Cryptolepis sanguinolenta, and its broad spectrum of biological activities has been illuminated in past decades. In this study, neocryptolepine and its derivatives (1-49) were designed and synthesized from economical and readily available starting materials. Their structures were confirmed by proton nuclear magnetic resonance, carbon nuclear magnetic resonance, and mass spectrometry. The synthesized compounds were screened for their antifungal profile against six agriculturally important fungi Rhizoctonia solani, Botrytis cinerea (B. cinerea), Fusarium graminearum, Mycosphaerella melonis, Sclerotinia sclerotiorum, and Magnaporthe oryzae. The results of in vitro assay revealed that compounds 5, 21, 24, 35, 40, 45, and 47 presented remarkable antifungal activity against the fungi tested with EC50 values lower than 1 μg/mL. Significantly, compound 24 displayed the most effective inhibitory potency against B. cinerea (EC50 = 0.07 μg/mL), and the data from in vivo experiments revealed that compound 24 demonstrated comparable protective activity with the positive control boscalid. Preliminary mechanism studies indicated that compound 24 showed impressive spore germination inhibitory effectiveness and lower cytotoxicity than azoxystrobin, imparted on normal function of the cell membrane and cell wall, and arrested the normal function of the nucleus. Besides the excellent inhibitory activity against agriculturally important phytopathogenic fungi tested, the designed assemblage possesses several benefits with a high profile of variation in synthesized molecules, the ease of synthesis, and good cost-effectiveness of commercially available synthetic reagents, all of these have highlighted the potential worth of compound 24 as a new and highly efficient agricultural fungicide.

Facile synthesis of 1-Methyl-1 H -benzo[ b ]azepines from 1-methylquinolinium iodides and diazo(trimethylsilyl)methylmagnesium bromide

Morita, Mikio,Hari, Yoshiyuki,Aoyama, Toyohiko

experimental part, p. 4221 - 4227 (2011/02/22)

The reaction of diazo(trimethylsilyl)methylmagnesium bromide, TMSC(MgBr)N2, with 1-methylquinolinium iodides followed by sequential ring expansion using copper(I) chloride gives 1-methyl-3-(trimethylsilyl)-1H- benzo[b]azepines in moderate to go

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