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PENTACHLOROTHIOANISOLE is a chemical compound that is primarily used in the synthesis of arenethiols and arenethiolates, which are important intermediates in the production of agrochemicals and fungicides.

1825-19-0

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1825-19-0 Usage

Uses

Used in Agrochemical Industry:
PENTACHLOROTHIOANISOLE is used as a precursor for the synthesis of arenethiols and arenethiolates, which are key components in the development of agrochemicals. These compounds play a crucial role in enhancing crop protection and improving agricultural productivity.
Used in Fungicide Industry:
PENTACHLOROTHIOANISOLE is also utilized in the preparation of arenethiols and arenethiolates for use in fungicides. These compounds help in the development of effective antifungal agents that protect crops from various fungal diseases, ensuring a healthy and bountiful harvest.

Check Digit Verification of cas no

The CAS Registry Mumber 1825-19-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,2 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1825-19:
(6*1)+(5*8)+(4*2)+(3*5)+(2*1)+(1*9)=80
80 % 10 = 0
So 1825-19-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H3Cl5S/c1-13-7-5(11)3(9)2(8)4(10)6(7)12/h1H3

1825-19-0 Well-known Company Product Price

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  • Sigma-Aldrich

  • (33367)  Methyl-pentachlorophenylsulfide  PESTANAL®, analytical standard

  • 1825-19-0

  • 33367-100MG

  • 629.46CNY

  • Detail

1825-19-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,4,5-pentachloro-6-methylsulfanylbenzene

1.2 Other means of identification

Product number -
Other names PENTACHLOROTHIOANISOLE

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:1825-19-0 SDS

1825-19-0Relevant articles and documents

Co-C bond cleavage in the reactions of alkyl, benzyl and heteroaromaticmethyl cobaloximes with arene sulfenyl chloride: Homolytic and heterolytic pathways

Gupta,Dixit, Vandana,Das, Indira

, p. 49 - 58 (2007/10/03)

The reactions of arene sulfenyl chlorides, ArSCl, (Ar=Ph, C6Cl5, 2,4 (NO2)2C6H3) with organocobaloximes, RCo(dmgH)2Py, (R=alkyl, benzyl and heteroaromaticmethyl) were carried out under thermal and photochemical conditions. A variety of organic and organometallic products are formed depending upon the substrate cobaloxime. For 3-methoxybenzyl and heteroaromaticmethyl cobaloximes the results suggest that they represent a unique class of cobaloximes whereby both the aromatic ring as well as the Co-C bond are highly activated towards attack by the arene sulfenyl chloride. Both homolytic as well as heterolytic pathways are operative.

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