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2584-46-5

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2584-46-5 Usage

Derivative of

Quinoline

Functional group

Thione

Common uses

a. Corrosion inhibitor
b. Intermediate in the synthesis of pharmaceuticals and agrochemicals
c. Manufacture of dyes
d. Manufacture of rubber chemicals

Chelating agent

Forms stable complexes with metal ions

Effective as a corrosion inhibitor

Due to its thione group and ability to chelate with metal ions

Versatile chemical properties

Potential applications in various industries

Check Digit Verification of cas no

The CAS Registry Mumber 2584-46-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,8 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2584-46:
(6*2)+(5*5)+(4*8)+(3*4)+(2*4)+(1*6)=95
95 % 10 = 5
So 2584-46-5 is a valid CAS Registry Number.

2584-46-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-dimethylquinoline-2-thione

1.2 Other means of identification

Product number -
Other names 1,4-Dimethyl-2-thiochinolon

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:2584-46-5 SDS

2584-46-5Downstream Products

2584-46-5Relevant articles and documents

Selenium Dioxide Oxidation of Alkylcoumarins and Related Methyl-Substituted Heteroaromatics

Ito, Kiichi,Nakajima, Kaoru

, p. 511 - 515 (2007/10/02)

By the use of selenium dioxide as the specific oxidizing agent in the coumarin series, the 4-ethyl, 4-propyl and 4-benzyl substituents of coumarin were converted into α-alcohols 2 and/or ketones 3, while 3-methyl- and 3-benzylcoumarins were converted into 3-acyl derivatives 7.The methyl substituent of the analogous thiocoumarin 5, chromones 10 or thiochromone 11 was also oxidized into the formyl functionality.Facile oxidative desulfurization into the ketone functionality, prior to methyl oxidation, was observed for the thione derivatives of 1a, 5, 6 and 10.

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