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204587-07-5

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204587-07-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 204587-07-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,4,5,8 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 204587-07:
(8*2)+(7*0)+(6*4)+(5*5)+(4*8)+(3*7)+(2*0)+(1*7)=125
125 % 10 = 5
So 204587-07-5 is a valid CAS Registry Number.

204587-07-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-N-(2-methylquinolin-4-yl)acetamide

1.2 Other means of identification

Product number -
Other names -

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:204587-07-5 SDS

204587-07-5Downstream Products

204587-07-5Relevant articles and documents

Lanthanide macrocyclic quinolyl conjugates as luminescent molecular-level devices

Gunnlaugsson,Mac Donaill,Parker

, p. 12866 - 12876 (2001)

The Eu(III) tetraazamacrocyclic complexes [Eu·1] and [Eu·2], and the Tb(III) and Yb(III) complexes [Tb·1] and [Yb·2], have been synthesized as luminescent molecular-level devices. The Eu complexes exhibit unique dual pH switching behavior in water under ambient conditions. The delayed Eu emission is reversibly switched on in acid, with an enhancement factor of several hundred for [Eu·1). These observations are consistent with the protonation of the quinoline aryl nitrogen moiety (pKa ≈ 5.9 for [Eu·1]). The fluorescence emission spectra of these complexes are unaffected by acid, but pronounced changes occur in alkaline solution due to the deprotonation of the aryl amide nitrogen (pKa ≈ 9.4 for [Eu·1]). [Tb·1] shows a more intriguing pH dependence; Tb emission is switched on only in the presence of H+ and in the absence of molecular oxygen, whereas the fluorescence emission properties are similar to those observed with [Eu·1). This behavior can be conveniently described as a molecular-level logic gate, corresponding to a two-input INHIBIT function, A λ B′. The analogous [Yb·2] complex shows no such pH or O2 dependence.

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