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4,6-Pyrimidinedicarboxaldehyde, 2-phenyl-, bis(methyl-2-pyridinylhydrazone) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

915135-35-2

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915135-35-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 915135-35-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,5,1,3 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 915135-35:
(8*9)+(7*1)+(6*5)+(5*1)+(4*3)+(3*5)+(2*3)+(1*5)=152
152 % 10 = 2
So 915135-35-2 is a valid CAS Registry Number.

915135-35-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenylpyrimidine-4,6-dicarbaldehyde bis[N-methyl-N-(pyridin-2-yl)hydrazone]

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:915135-35-2 SDS

915135-35-2Downstream Products

915135-35-2Relevant academic research and scientific papers

Electronic absorption and emission properties of bishydrazone [2?×?2] metallosupramolecular grid-type architectures

Holub, Jan,Santoro, Antonio,Lehn, Jean-Marie

, p. 223 - 231 (2019/06/07)

Several ditopic ligands containing two tridentate bishydrazone coordination subunits and their Zn(II) and Cd(II) [2 × 2] grid-type complexes were prepared and their photoluminescent properties studied. A special attention was devoted to the influence of the orientation of the hydrazone group N–N[dbnd]in the core of the ligands and their complexes. Its reversal from [pyridine[dbnd]N–N–pyrimidine] (L1) to [pyridine–N–N[dbnd]pyrimidine] (L2) has a strong impact on the observed absorption and emission behaviour of particular ligands (L1 and L2) as well as of their [2 × 2] grid assemblies. The further lateral functionalization of the ligands led to different emission quantum yields of the resulting grids, while their emission and absorption spectra varied very little. The simplest derivative L1 turned out to have the best performance with, for its Zn(II) complex, relatively high quantum yield 60%.

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