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2-methoxy-4-[(E)-2-(1-methyl-1,2-dihydropyridin-2-yl)ethenyl]phenol is a complex organic compound with a molecular formula of C18H19NO2. It is characterized by a phenol group (C6H5OH) with a methoxy (-OCH3) substituent at the 2nd position and a (E)-2-(1-methyl-1,2-dihydropyridin-2-yl)ethenyl group attached at the 4th position. The 1,2-dihydropyridine ring is a six-membered nitrogen-containing ring with a double bond between the 2nd and 3rd carbon atoms, and a methyl group attached to the nitrogen atom. 2-methoxy-4-[(E)-2-(1-methyl-1,2-dihydropyridin-2-yl)ethenyl]phenol is likely to be found in the field of pharmaceuticals or as an intermediate in the synthesis of various chemical compounds due to its unique structure and potential reactivity.

5418-67-7

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5418-67-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5418-67-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,1 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5418-67:
(6*5)+(5*4)+(4*1)+(3*8)+(2*6)+(1*7)=97
97 % 10 = 7
So 5418-67-7 is a valid CAS Registry Number.

5418-67-7SDS

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-methoxy-4-[(Z)-2-(1-methylpyridin-1-ium-2-yl)ethenyl]phenol,iodide

1.2 Other means of identification

Product number -
Other names 2-(4-hydroxy-3-methoxy-trans-styryl)-1-methyl-pyridinium,iodide

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:5418-67-7 SDS

5418-67-7Downstream Products

5418-67-7Relevant academic research and scientific papers

Dual spectroscopic responses of pyridinium hemicyanine dyes to anions

Xie, Puhui,Guo, Fengqi,Zhang, Dasheng,Zhang, Lei

experimental part, p. 1975 - 1981 (2012/07/14)

The absorption and fluorescence spectroscopic responses of three pyridinium hemicyanine dyes to anions F-, Cl-, Br-, I-, H2PO4-, HSO4 - and OAc- were investigated. At lower concentrations of OAc- (less than 1 equiv.), both the absorption and the fluorescence intensities of 1-3 were more effectively changed than F- at identical concentrations. At higher concentrations of OAc- (more than 1 equiv.), the interaction was opposite for each compound. 1H NMR results indicated the interaction between 1, 2 or 3 and F- proceeded through hydrogen bonding. The results showed that these dyes are promising to develop dual fluorescence and chromogenic chemosensors toward F- and OAc- according to the subtle difference in the affinity of F - and OAc-. Pyridinium hemicyanine dyes bearing hydroxyl groups on the benzene ring provide a simple class of anion receptors which are capable of selectively reporting the presence of F- and OAc - in CH3CN by color changes. Copyright

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