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21225-59-2

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21225-59-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21225-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,2,2 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 21225-59:
(7*2)+(6*1)+(5*2)+(4*2)+(3*5)+(2*5)+(1*9)=72
72 % 10 = 2
So 21225-59-2 is a valid CAS Registry Number.

21225-59-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-diacetyl-4-phenylheptane-2,6-dione

1.2 Other means of identification

Product number -
Other names 3,5-Diacetyl-4-phenyl-heptandion-(2,6)

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:21225-59-2 SDS

21225-59-2Relevant articles and documents

Syntheses, solvatochromism, and antimicrobial activities of new binuclear copper(II) mixed-ligand complexes in a ternary system with β-diketones and diamine ligands

Abou-Hussein,Mahmoud, Nelly H.,Linert, Wolfgang

experimental part, p. 2592 - 2605 (2011/12/04)

Ternary complexes of binuclear copper(II) nitrate with bis(β- diketones) [β-diketones = 2-phenyl-1,3-bis-(tetraacetyl-propane), L 1, or 2-(o-hydroxyphenyl-1,3-bis-(tetraacetyl-propane), L 2] and diamines [diamines = N,N,N′,N′- tetramethylethylenediamine (tmen), 2,2′-bipyidine (bipy) and 1,10-phenanthroline (phen)] have been synthesized, where [image omitted] groups are counter or coordinated anions. The structures of the complexes and their solvatochromic behavior were investigated by elemental analysis, spectroscopic, magnetic, molar conductance, and thermal analysis. Solvatochromism was observed for only three complexes where they displayed a drastic color change with increasing donor strength of the solvent. This behavior is due to the solute-solvent interaction between the chelate cation and the solvent. Spectroscopic studies of the complexes implicate tetragonal distortions in strongly polar solvents and square planar or square pyramidal geometries in the presence of weakly coordinating molecules. Biological studies of the ligands and their complexes showed a significant inhibition on the growth of selected Gram-positive bacteria and moderate effect against two kinds of Gram-negative bacteria as well as one kind of pathogenic fungi.

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