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210096-14-3

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210096-14-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 210096-14-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,0,0,9 and 6 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 210096-14:
(8*2)+(7*1)+(6*0)+(5*0)+(4*9)+(3*6)+(2*1)+(1*4)=83
83 % 10 = 3
So 210096-14-3 is a valid CAS Registry Number.

210096-14-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-anthracen-9-yl-2-hydroxybenzaldehyde

1.2 Other means of identification

Product number -
Other names 3-anthracenyl-2-hydroxybenzaldehyde

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:210096-14-3 SDS

210096-14-3Downstream Products

210096-14-3Relevant articles and documents

Synthesis and photochemical behaviour of novel uranyl-salophen complexes bearing anthracenyl side arms

Mihan, Francesco Yafteh,Bartocci, Silvia,Credi, Alberto,Silvi, Serena,Dalla Cort, Antonella

, p. 109 - 115 (2013/08/24)

In this paper, we report the synthesis and physico-chemical investigation of two uranyl-salophen receptors, bearing either one or two anthracenyl moieties appended to the salophen skeleton. Despite the presence of the anthracenyl fluorophores, no fluorescence emission was detected. Photophysical data and cyclic voltammetric experiments show that photoinduced electron transfer from the anthracene-localised first singlet excited state to the metal centre is strongly exergonic, thus suggesting that this is the main fluorescence quenching mechanism in these complexes. The investigated compounds are photoreactive upon UV irradiation, yielding either anthracene photooxidation or photodimerisation products depending on the specific complex and the experimental conditions.

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