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1124-07-8

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1124-07-8 Usage

General Description

4,6-dichloro-m-cresol, also known as Canertinib, is a chemical compound with the molecular formula C7H6Cl2O. Notably, it is an organic compound which belongs to the family of phenols, specifically the class of dichlorophenols. 4,6-dichloro-m-cresol is best characterised by its distinctive properties, which include a faint aromatic smell and a white crystalline appearance. In terms of application, it is principally used as a fungicide in agriculture and in certain healthcare products. One of its notable features is its ability to eliminate fungi and mould which can heavily contaminate crops and slow or halt their growth. However, it being a toxic compound, it may lead to health problems if inhaled, consumed or comes into contact with skin, and it's also harmful to the environment. It is listed as a hazardous substance under multiple regulations worldwide, hence requiring careful handling and disposal.

Check Digit Verification of cas no

The CAS Registry Mumber 1124-07-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1124-07:
(6*1)+(5*1)+(4*2)+(3*4)+(2*0)+(1*7)=38
38 % 10 = 8
So 1124-07-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H6Cl2O/c1-4-2-7(10)6(9)3-5(4)8/h2-3,10H,1H3

1124-07-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-Dichloro-5-methylphenol

1.2 Other means of identification

Product number -
Other names 2,4-dichloro-5-methyl-phenol

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:1124-07-8 SDS

1124-07-8Relevant articles and documents

Investigations of the reactions of monochloramine and dichloramine with selected phenols: Examination of humic acid models and water contaminants

Heasley, Victor L.,Fisher, Audra M.,Herman, Erica E.,Jacobsen, Faith E.,Miller, Evan W.,Ramirez, Ashley M.,Royer, Nicole R.,Whisenand, Josh M.,Zoetewey, David L.,Shellhamer, Dale F.

, p. 5022 - 5029 (2008/04/18)

The phenols are an important area of investigation because they are substituents in the humic acids and are common contaminants in water. The reactivities and orientations of two common phenols (phenol and m-cresol), and some of their chlorinated intermediates with aqueous monochloroamine and dichloroamine were presented. m-Cresol was more reactive than phenol with both chlorinating agents. NH2Cl and NHCl2 showed extensive reactivity toward the phenols, even the partially chlorinated less reactive intermediates would be expected to fully chlorinate the activated positions in phenolic substituents in the humic acids.

HIGH SITE-SELECTIVITY IN THE CHLORINATION OF ELECTRON-RICH AROMATIC COMPOUNDS BY N-CHLORAMMONIUM SALTS.

Smith, John R. Lindsay,McKeer, Linda C.

, p. 3117 - 3120 (2007/10/02)

N-Chlorammonium salts are efficient and very site-selective monochlorinating agents for electron-rich aromatic compounds.

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