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54120-68-2

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54120-68-2 Usage

General Description

2-(4-Pyridinyl)-2-oxazoline is a chemical compound that belongs to the class of oxazolines, which are five-membered heterocyclic compounds containing oxygen and nitrogen atoms. It is also known as 4-pyridyl-2-oxazoline and has the molecular formula C7H7NO. 2-(4-Pyridinyl)-2-oxazoline is commonly used as a ligand in organometallic chemistry and catalysis due to its ability to coordinate with metal atoms. It can also act as a chelating agent, forming stable complexes with metal ions. Additionally, 2-(4-Pyridinyl)-2-oxazoline has been studied for its potential biological activities, including antimicrobial, anti-inflammatory, and anticancer properties. Overall, this compound has diverse applications in various fields, making it a valuable and versatile chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 54120-68-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,1,2 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 54120-68:
(7*5)+(6*4)+(5*1)+(4*2)+(3*0)+(2*6)+(1*8)=92
92 % 10 = 2
So 54120-68-2 is a valid CAS Registry Number.

54120-68-2SDS

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 2-pyridin-4-yl-4,5-dihydro-1,3-oxazole

1.2 Other means of identification

Product number -
Other names 4-(2-oxazolinyl)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:54120-68-2 SDS

54120-68-2Relevant articles and documents

Synthetic use of the primary kinetic isotope effect in hydrogen atom transfer: Generation of α-aminoalkyl radicals

Wood, Mark E.,Bissiriou, Sabine,Lowe, Christopher,Norrish, Andrew M.,Senechal, Katell,Windeatt, Kim M.,Coles, Simon J.,Hursthouse, Michael B.

experimental part, p. 4653 - 4665 (2010/11/17)

The extent to which deuterium can act as a protecting group to prevent unwanted 1,5-hydrogen atom transfer to aryl and vinyl radical intermediates was examined in the context of the generation of α-aminoalkyl radicals in a pyrrolidine ring. Intra- and int

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