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13362-75-9

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13362-75-9 Usage

Description

(E)-2-[2-(3-pyridyl)vinyl]pyridine, also known as 2-(3-pyridyl)ethenylpyridine, is a chemical compound with the molecular formula C12H9N. It is a yellow crystalline solid with a characteristic odor. (E)-2-[2-(3-pyridyl)vinyl]pyridine is recognized for its potential applications in the development of new drugs and materials, as well as its ability to act as a ligand in coordination chemistry and as a precursor for the synthesis of various organic compounds. Its unique and versatile chemical properties make it a valuable component in the field of chemical research and industry.

Uses

Used in Organic Synthesis:
(E)-2-[2-(3-pyridyl)vinyl]pyridine is used as a building block for the synthesis of complex organic molecules. Its presence in the molecular structure allows for the creation of a wide range of compounds with diverse properties and potential applications.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (E)-2-[2-(3-pyridyl)vinyl]pyridine is used as a key component in the development of new drugs. Its unique chemical properties enable the design and synthesis of novel therapeutic agents with potential applications in various medical fields.
Used in Coordination Chemistry:
(E)-2-[2-(3-pyridyl)vinyl]pyridine is used as a ligand in coordination chemistry, where it forms complexes with metal ions. These complexes have potential applications in catalysis, materials science, and as models for understanding biological processes.
Used as a Precursor for Synthesis:
(E)-2-[2-(3-pyridyl)vinyl]pyridine serves as a precursor for the synthesis of various organic compounds, contributing to the development of new materials and chemicals with specific properties and functions.

Check Digit Verification of cas no

The CAS Registry Mumber 13362-75-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,6 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13362-75:
(7*1)+(6*3)+(5*3)+(4*6)+(3*2)+(2*7)+(1*5)=89
89 % 10 = 9
So 13362-75-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H10N2/c1-2-9-14-12(5-1)7-6-11-4-3-8-13-10-11/h1-10H/b7-6+

13362-75-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-1-(2-pyridyl)-2-(3-pyridyl)ethylene

1.2 Other means of identification

Product number -
Other names .2,3'-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:13362-75-9 SDS

13362-75-9Relevant articles and documents

Palladium- meta -terarylphosphine catalyst for the Mizoroki-Heck reaction of (hetero)aryl bromides and functional olefins

Tay, Daniel Weiliang,Jong, Howard,Lim, Yee Hwee,Wu, Wenqin,Chew, Xinying,Robins, Edward G.,Johannes, Charles W.

, p. 4054 - 4063 (2015/05/05)

The evolutionary meta-terarylphosphine ligand architecture of Cy?Phine was recently shown to be a key feature that imposed outstanding performance in palladium-catalyzed copper-free Sonogashira applications. Herein, the Pd-Cy?Phine combination has similar

Heck cross-coupling of vinyl heteroaromatic compounds with aryl and heteroaryl halides using Pd(II) complex under phosphine-free conditions

Annapurna, Manne,Vishnuvardhan Reddy,Singh, Surya Prakash,Kantam, Mannepalli Lakshmi

, p. 10940 - 10945 (2014/01/06)

The palladium-catalyzed cross-coupling reaction of vinyl heteroaromatic compounds with aryl bromides and heteroaryl bromides is described using air and moisture stable N,N′,N″,O-tetrafunctional Pd catalyst under phosphine-free conditions. As a result a variety of trans-1,2-disubstituted vinyl heterocycles were obtained in high to good yields.

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