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Pyridine, 4-[(1E)-2-phenylethenyl]-, hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19337-93-0

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19337-93-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19337-93-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,3,3 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19337-93:
(7*1)+(6*9)+(5*3)+(4*3)+(3*7)+(2*9)+(1*3)=130
130 % 10 = 0
So 19337-93-0 is a valid CAS Registry Number.

19337-93-0SDS

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 4-(2-phenylethenyl)pyridine,hydrochloride

1.2 Other means of identification

Product number -
Other names 4-trans-Styryl-pyridin,Hydrochlorid

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:19337-93-0 SDS

19337-93-0Upstream product

19337-93-0Relevant academic research and scientific papers

Role of hydrogen bonds in molecular packing of photoreactive crystals: Templating photodimerization of protonated stilbazoles in crystalline state with a combination of water molecules and chloride ions

Mondal, Barnali,Zhang, Tingting,Prabhakar, Rajeev,Captain, Burjor,Ramamurthy

, p. 1509 - 1520 (2014/12/10)

A difference in photobehavior and molecular packing between hydrated and anhydrous crystals of protonated trans-stilbazoles has been identified. While stilbazoles are not photoreactive in the crystalline state, upon protonation with HCl in the solid state they dimerized to a single dimer (anti-head-tail) when exposed to UV light. In these photoreactive crystals the protonated stilbazole molecules are arranged in a ladder-like format with the rungs made up of water molecules and chloride ions. A combination of water and chloride ion holds the protonated trans-stilbazoles through either N-H...O or N-H...Cl- interactions. Anhydrous protonated stilbazole crystals prepared by heating the 'wet' crystals under reduced pressure were inert upon exposure to UV light. As per X-ray crystal structure analyses these light stable crystals did not contain water molecules in their lattice. The current investigation has established that water molecules are essential for photodimerization of crystalline protonated trans-stilbazoles. To compare the reactivity of protonated trans-stilbazoles with that of protonated cis-stilbazoles, photoreactivity and packing arrangement of cis-4-iodo stilbazole?HCl salt was examined. This molecule in the crystalline state only isomerized to the trans isomer and did not dimerize. Thus, while the trans isomer dimerized and did not isomerize, the cis isomer only isomerized and did not dimerize in the crystalline state. To probe the role of cation...π interaction in the packing of protonated trans-stilbazoles, energies of various types of packing in the gas phase were estimated by MP-2 calculations and cation...π interaction was found to be unimportant in the packing of protonated trans-stilbazole crystals investigated here.

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