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67525-28-4

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67525-28-4 Usage

General Description

2-Chloro-3-ethylquinoline is a chemical compound with the molecular formula C11H10ClN. It is a quinoline derivative with a chloro substituent at the 2 position and an ethyl group at the 3 position. 2-CHLORO-3-ETHYLQUINOLINE is used as a building block in organic synthesis and pharmaceutical research. It has been studied for its potential biological activities, including its antibacterial and antimalarial properties. 2-Chloro-3-ethylquinoline may also have applications in the development of new drugs and agrochemicals. Overall, it is a versatile chemical that has potential in various scientific and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 67525-28-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,5,2 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 67525-28:
(7*6)+(6*7)+(5*5)+(4*2)+(3*5)+(2*2)+(1*8)=144
144 % 10 = 4
So 67525-28-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H10ClN/c1-2-8-7-9-5-3-4-6-10(9)13-11(8)12/h3-7H,2H2,1H3

67525-28-4 Well-known Company Product Price

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  • Aldrich

  • (BBO000255)  2-Chloro-3-ethylquinoline  AldrichCPR

  • 67525-28-4

  • BBO000255-1G

  • 2,575.17CNY

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67525-28-4SDS

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-CHLORO-3-ETHYLQUINOLINE

1.2 Other means of identification

Product number -
Other names 3-Aethyl-2-chlor-chinolin

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:67525-28-4 SDS

67525-28-4Relevant articles and documents

Iron-Catalyzed Amination of Strong Aliphatic C(sp3)-H Bonds

Das, Sandip Kumar,Roy, Satyajit,Khatua, Hillol,Chattopadhyay, Buddhadeb

, p. 16211 - 16217 (2020/10/26)

A concept for intramolecular denitrogenative C(sp3)-H amination of 1,2,3,4-tetrazoles bearing unactivated primary, secondary, and tertiary C-H bonds is discovered. This catalytic amination follows an unprecedented metalloradical activation mechanism. The utility of the method is showcased with the short synthesis of a bioactive molecule. Moreover, an initial effort has been embarked on for the enantioselective C(sp3)-H amination through the catalyst design. Collectively, this study underlines the development of C(sp3)-H bond functionalization chemistry that should find wide application in the context of drug discovery and natural product synthesis.

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