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1-(-2-PYRIDYL)-2-(4-PYRIDYL)ETHYLENE is a symmetrical organic compound characterized by the molecular formula C13H10N2. It features two pyridine rings linked by an ethylene bridge, offering a unique structure that is valuable in the synthesis of other organic compounds. 1-(-2-PYRIDYL)-2-(4-PYRIDYL)ETHYLENE is recognized for its potential applications in pharmaceutical and material science research, as well as its utility as a building block for developing new chemical compounds with tailored functions and properties. Its versatility and structural attributes also suggest possible uses in the creation of advanced materials for electronics, optics, and other technological applications.

14802-41-6

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14802-41-6 Usage

Uses

Used in Pharmaceutical Research:
1-(-2-PYRIDYL)-2-(4-PYRIDYL)ETHYLENE is used as a key intermediate in the synthesis of pharmaceutical compounds for various therapeutic applications. Its unique structure allows for the development of new drugs with specific targeting and activity profiles, contributing to advancements in medicinal chemistry.
Used in Material Science Research:
In the field of material science, 1-(-2-PYRIDYL)-2-(4-PYRIDYL)ETHYLENE is utilized as a component in the design and synthesis of new materials with specialized properties. Its incorporation into material formulations can lead to the creation of innovative products with applications in various industries.
Used in Electronics Industry:
1-(-2-PYRIDYL)-2-(4-PYRIDYL)ETHYLENE is used as a component in the development of electronic materials, potentially enhancing the performance of electronic devices through its incorporation into semiconductors, conductors, or other electronic components.
Used in Optics Industry:
1-(-2-PYRIDYL)-2-(4-PYRIDYL)ETHYLENE is also used in the optics industry, where it may contribute to the development of new optical materials with improved light transmission, reflection, or other optical properties, thus advancing optical technologies.
Used in Chemical Compound Development:
1-(-2-PYRIDYL)-2-(4-PYRIDYL)ETHYLENE serves as a building block for the creation of new chemical compounds with specific functions and properties, expanding the scope of chemical research and innovation.

Check Digit Verification of cas no

The CAS Registry Mumber 14802-41-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,8,0 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14802-41:
(7*1)+(6*4)+(5*8)+(4*0)+(3*2)+(2*4)+(1*1)=86
86 % 10 = 6
So 14802-41-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H10N2/c1-2-8-14-12(3-1)5-4-11-6-9-13-10-7-11/h1-10H/b5-4+

14802-41-6SDS

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-(2-pyridin-4-ylethenyl)pyridine

1.2 Other means of identification

Product number -
Other names 2,4'-ethene-1,2-diyl-bis-pyridine

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:14802-41-6 SDS

14802-41-6Upstream product

14802-41-6Relevant academic research and scientific papers

Utilities of olefin derivatives

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Page/Page column 20; 30, (2008/06/13)

Compounds having an activity to enhance the expression of apoAI are provided. Compounds of formula (I): in which Ar1 and Ar2 are independently a phenyl, naphthyl, or monocyclic or bicyclic aromatic heterocyclic group, which may be optionally substituted; —X— is —N═CZ2-, —CY2═CZ2-, —CY2Y3—CHZ2-, —S—, —O—, or the like; Y1, Y2, Y3, Z1 and Z2 are independently a hydrogen, a halogen, a lower alkyl, a phenyl, or the like; Z1 and Z2 may be independently a linker group that may combine with Ar2 and Ar1 to form a condensed ring; m is 0 or 1, and n is 0 to 2; a prodrug thereof, a pharmaceutically acceptable salt or solvate of them; are disclosed.

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