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S-[2-(4-bromophenyl)-2-oxoethyl] O-propan-2-yl carbonodithioate is a complex organic chemical compound with the molecular formula C11H12BrOS2. It is a colorless to pale yellow solid and is primarily used as a pesticide, specifically as an acaricide, to control mites and ticks in agriculture. S-[2-(4-bromophenyl)-2-oxoethyl] O-propan-2-yl carbonodithioate is known for its effectiveness in managing pest populations and is often used in integrated pest management strategies. It is important to note that, like many pesticides, it must be handled with care due to its potential toxicity and should be used in accordance with safety guidelines and regulations to minimize environmental and health risks.

1861-49-0

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1861-49-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1861-49-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,6 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1861-49:
(6*1)+(5*8)+(4*6)+(3*1)+(2*4)+(1*9)=90
90 % 10 = 0
So 1861-49-0 is a valid CAS Registry Number.

1861-49-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name O-propan-2-yl [2-(4-bromophenyl)-2-oxoethyl]sulfanylmethanethioate

1.2 Other means of identification

Product number -
Other names O-Isopropyl-S-(p-bromphenacyl)-dithiocarbonat

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:1861-49-0 SDS

1861-49-0Relevant academic research and scientific papers

Flexible routes to thiophenes

Jullien, Helene,Quiclet-Sire, Beatrice,Tetart, Thomas,Zard, Samir Z.

supporting information, p. 302 - 305 (2014/01/23)

Three convergent routes to thiophenes are described, hinging on the radical addition of α-xanthyl ketones to ethyl vinyl sulfide or to vinyl pivalate. The latter route ultimately proved to be the most versatile and efficient (61-94%).

SYNTEZY ZWIAZKOW O POTENCJALNYM DZIALANIU RADIOUCZULAJACYM. VIII. SYNTEZY ALKILOKSANTOGENIANOW 4-CHLORO- I 4-BROMOFENACYLOWYCH

Skwarski, Dionizy,Sobolewski, Henryk

, p. 213 - 218 (2007/10/02)

In the frame-work of search for new potential radiosensitizers a series of novel 4-chloro- and 4-bromophenacyl alkylxanthates were synthetized by reacting 4-chloro- and 4-bromophenacyl bromide with potassium alkylxanthates, in which allyl, ethyl, propyl, isopropyl, butyl, isobutyl, pentyl, isopentyl, heksyl, heptyl, octyl, isooctyl, decyl, 3-tetrahydrofurfuryl, benzyl, phenylethyl and phenylpropyl constituted the alkyl group.

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