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109297-66-7

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109297-66-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109297-66-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,2,9 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 109297-66:
(8*1)+(7*0)+(6*9)+(5*2)+(4*9)+(3*7)+(2*6)+(1*6)=147
147 % 10 = 7
So 109297-66-7 is a valid CAS Registry Number.

109297-66-7SDS

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 2-[anthracen-9-ylmethyl(2-hydroxyethyl)amino]ethanol

1.2 Other means of identification

Product number -
Other names Ethanol,2,2'-[(9-anthracenylmethyl)imino]bis

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:109297-66-7 SDS

109297-66-7Downstream Products

109297-66-7Relevant articles and documents

Detection of hydrogen peroxide using dioxazaborocanes: elucidation of the sensing mechanism at the molecular level by NMR and XPS measurements

Caron, Thomas,Palmas, Pascal,Frénois, Céline,Méthivier, Christophe,Pasquinet, Eric,Pradier, Claire-Marie,Serein-Spirau, Fran?oise,Hairault, Lionel,Montméat, Pierre

, p. 4114 - 4121 (2020/03/19)

A fluorescent dioxazaborocane was synthesised and characterized, in order to study its turn-off sensing process for hydrogen peroxide detection. The exposure of the dioxazaborocane to diluted vapours of H2O2 led to a strong non reversible quenching of the fluorescence. Both NMR and XPS analyses were carried out before and after exposure of dioxazaborocane to H2O2 vapours. They unequivocally show that the boron atom is oxidised in the film with cleavage of the N-B dative bond. Identification of products such as phenol and boric acid by NMR, supported by consistent XPS data, enabled the whole reaction sequence that explains the fluorescence quenching of dioxazaborocane upon H2O2 exposure to be described accurately. Direct hydrolysis of dioxazaborocane to diol, without oxidation, was only marginally observed.

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