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15407-92-8

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15407-92-8 Usage

Derived from

Pyridine group

Structure

Phenol ring with an attached dihydropyridine group

Configuration

Trans configuration in the dihydropyridine moiety

Usage

Research reagent

Potential applications

Pharmaceutical industry

Suitability

Further study in medicinal chemistry and drug development

Check Digit Verification of cas no

The CAS Registry Mumber 15407-92-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,0 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15407-92:
(7*1)+(6*5)+(5*4)+(4*0)+(3*7)+(2*9)+(1*2)=98
98 % 10 = 8
So 15407-92-8 is a valid CAS Registry Number.

15407-92-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(E)-2-(1-methylpyridin-1-ium-2-yl)ethenyl]phenol,iodide

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:15407-92-8 SDS

15407-92-8Downstream Products

15407-92-8Relevant articles and documents

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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