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1-Azoniabicyclo[2.2.2]octane, 3-hydroxy-1-(phenylmethyl)-, bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

203335-99-3

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203335-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 203335-99-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,3,3,3 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 203335-99:
(8*2)+(7*0)+(6*3)+(5*3)+(4*3)+(3*5)+(2*9)+(1*9)=103
103 % 10 = 3
So 203335-99-3 is a valid CAS Registry Number.

203335-99-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-1-azoniabicyclo[2.2.2]octan-3-ol,bromide

1.2 Other means of identification

Product number -
Other names AmbscCN4/4088

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:203335-99-3 SDS

203335-99-3Downstream Products

203335-99-3Relevant academic research and scientific papers

Directing Aluminum Atoms into Energetically Favorable Tetrahedral Sites in a Zeolite Framework by Using Organic Structure-Directing Agents

Muraoka, Koki,Chaikittisilp, Watcharop,Yanaba, Yutaka,Yoshikawa, Takeshi,Okubo, Tatsuya

, p. 3742 - 3746 (2018)

The Al location in zeolites can have massive influences on the zeolite properties because it directly correlates with the cationic active sites. Herein, the synthesis of IFR zeolites with controlled Al distribution at different tetrahedral sites (T sites)

Quaternary salts derived from 3-substituted quinuclidine as potential antioxidative and antimicrobial agents

Od?ak, Renata,?prung, Matilda,Soldo, Barbara,Sko?ibu?i?, Mirjana,Gudelj, Martina,Mui?, Anita,Primo?iènes, Ines

, p. 320 - 331 (2017)

Two series of novel ammonium salts containing the quinuclidine moiety were prepared in order to evaluate their antioxidative, antibacterial and antifungal potential. The synthesized homologues of 3-hydroxy (QOH) and 3-chloroquinuclidine (QCl) with the different N-benzyl substituents at the para-position (bromo, chloro or nitro group) were obtained in very good yields and characterized by IR and NMR spectroscopies and elemental analysis. All compounds were tested for antioxidative activity using the oxygen radical absorbance capacity (ORAC) assay and among tested samples, N-p-nitrobenzyl-3-hydroxyquinuclidinium bromide (QOH-4) exhibited the highest antioxidative potential (293.80 nmol (TE) mL-1), which was further investigated by the DNA nicking assay. The biological activity of selected compounds was evaluated by measuring the zone of inhibition and by determining the minimal inhibitory concentration (MIC) against three Gram-positive bacteria (B. cereus, E. faecalis and S. aureus), three Gram-negative bacteria (E. coli, P. aeruginosa and C. sakazakii) and three fungi species (C. albicans, A. Niger and P. notatum). The bioactivity assay showed that some newly synthetized quaternary quinuclidinium compounds display a comparable or even better antibacterial and antifungal activity than the reference drugs such as gentamicin (GEN), cefotaxime (CTX) and amphotericin B (AMPHB). Among the tested compounds, N-p-chlorobenzyl-3-hydroxyquinuclidinium bromide (QOH-3) exhibited a considerable antibacterial efficiency against P. aeruginosa (MIC=0.39 μg mL-1) and QOH-4 displayed a potent antifungal activity against C. albicans (MIC=1.56 μg mL-1).

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