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25351-57-9

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25351-57-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25351-57-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,3,5 and 1 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 25351-57:
(7*2)+(6*5)+(5*3)+(4*5)+(3*1)+(2*5)+(1*7)=99
99 % 10 = 9
So 25351-57-9 is a valid CAS Registry Number.

25351-57-9SDS

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 (E)-3-phenyl-N-[3-[[(E)-3-phenylprop-2-enylidene]amino]propyl]prop-2-en-1-imine

1.2 Other means of identification

Product number -
Other names N1,N3-Bis(3-phenyl-2-propenylidene)-1,3-propanediamine

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:25351-57-9 SDS

25351-57-9Downstream Products

25351-57-9Relevant articles and documents

Investigation of complexation behavior of the dithiocarbamates of N1,Nn-dicinnamylalkane-1,n-diamines with metals

Halimehjani, Azim Ziyaei,Movahed, Farzaneh Soleymani,Fathi, Mohammad B.,Daliri, Rasoul,Saidi, Mohammad R.

, p. 188 - 195 (2019)

Synthesis and characterization of metal dithiocarbamate complexes of N1,N3-dicinnamylpropane-1,3-diamine, N1,N4-dicinnamylbutane-1,4-diamine and N1,N6-dicinnamylhexane-1,6-diamine are reported. The ligands are prepared using cinnamaldehyde and primary diamines to provide the corresponding diimines, followed by reduction with NaBH4 to afford the corresponding secondary diamines. Diamines react with carbon disulfide in basic medium to furnish the corresponding bis(dithiocarbamate) salts, which underwent complexation with metals. The prepared complexes were characterized by IR, 1H and 13C NMR, TGA and elemental analyses. Although the dinuclear metal dithiocarbamate macrocyclic complexes were obtained from N1,N6-dicinnamylhexane-1,6-diamine, the propane and butane diamines afforded the corresponding polymers. The synthesized complexes do not show any crystalline phase even in long lasting terms. Electron microscopy obviously shows that the material is amorphous, and X-ray diffraction technique is employed to investigate atom-atom distances in the molecule via the Fourier transform analysis of XRD data collected from powder sample.

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