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Pyridine, 3-[(1E,3Z)-4-phenyl-1,3-butadienyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

473935-18-1

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473935-18-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 473935-18-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,3,9,3 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 473935-18:
(8*4)+(7*7)+(6*3)+(5*9)+(4*3)+(3*5)+(2*1)+(1*8)=181
181 % 10 = 1
So 473935-18-1 is a valid CAS Registry Number.

473935-18-1SDS

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 (1E,3Z)-1-(3-pyridyl)-4-(phenyl)buta-1,3-diene

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:473935-18-1 SDS

473935-18-1Relevant academic research and scientific papers

Photoisomerization mechanisms and photoselectivity of the stereoisomers of 1-(pyrid-n-yl),4-phenylbuta-1,3-diene

Bartocci,Galiazzo,Latterini,Marri,Mazzucato,Spalletti

, p. 2911 - 2916 (2007/10/03)

The positional isomers of 1-(pyrid-n-yl),4-phenylbuta-1,3-diene (n = 2, 3 and 4) have been synthesized and characterized by spectrometric techniques. All the four expected stereoisomers (EE, EZ, ZE and ZZ) were prepared for n = 2 while only three and two geometrical isomers were obtained for the positional isomers with n = 3 and 4, respectively. Their excited state properties were investigated by stationary and pulsed fluorimetric techniques and by laser flash photolysis. This paper describes the photochemical behaviour under direct and triplet sensitized excitation. The selective formation of photoproducts and the role of diabatic/adiabatic mechanisms are reported and compared with the results on the direct photoisomerization of the EE and ZE isomers in the singlet manifold described in a previous paper (G. Bartocci, G. Galiazzo, U. Mazzucato and A. Spalletti, Phys. Chem. Chem. Phys., 2001, 3, 379-386).

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