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1,2-dichloro-4-[3-methyl-4-(methylsulfonyl)phenoxy]benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83642-38-0

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83642-38-0 Usage

Chemical compound

Yes

Usage

Insecticide and acaricide in agricultural and horticultural settings

Mode of action

Interferes with the nervous system of pests, leading to their death

Toxicity to humans

Moderately toxic

Potential health effects

Skin and eye irritation upon contact

Safety precautions

Important to handle and use with proper safety measures to prevent harmful effects on human health and the environment

Check Digit Verification of cas no

The CAS Registry Mumber 83642-38-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,6,4 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 83642-38:
(7*8)+(6*3)+(5*6)+(4*4)+(3*2)+(2*3)+(1*8)=140
140 % 10 = 0
So 83642-38-0 is a valid CAS Registry Number.

83642-38-0SDS

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 4-(3,4-dichlorophenoxy)-2-methyl-1-methylsulfonylbenzene

1.2 Other means of identification

Product number -
Other names -

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:83642-38-0 SDS

83642-38-0Downstream Products

83642-38-0Relevant academic research and scientific papers

Sulfur-substituted diphenyl ethers having antiviral activity

-

, (2008/06/13)

Novel compounds exhibiting antiviral activity are disclosed, such compounds are represented by the formula: STR1 wherein m represents the integer 0, 1 or 2; R represents trihalomethyl, alkyl or phenyl; R1 represents hydrogen, bromo, chloro, fluoro, cyano, nitro, amino, alkyl, alkoxy or trifluoromethyl; R2 represents hydroxyl, bromo, chloro, fluoro, cyano, acetyl, benzoyl, substituted benzoyl, alkyl, alkoxy, substituted alkoxy, benzyl, substituted benzyl, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylaminosulfonyl, dialkylaminosulfonyl, or the radical --O(CH2)n R4 wherein n represents the integer 1, 2 or 3 and R4 represents cyano or dialkylamino; R3 represents hydrogen, hydroxyl, bromo, chloro, fluoro, cyano, acetyl, benzoyl, substituted benzoyl, alkyl, alkoxy, substituted alkoxy, benzyl, substituted benzyl, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylaminosulfonyl, dialkylaminosulfonyl, or the radical --O(CH2)n R4 wherein n represents the integer 1, 2 or 3; and R4 represents cyano or dialkylamino; or alternatively R2 and R3 taken together represent the radical --O--C(X)2 --O-- wherein X represents hydrogen, bromo, chloro or fluoro. Methods of using the above-noted compounds and structurally related compounds to employ their antiviral activity are also disclosed as well as pharmaceutically-acceptable compositions.

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