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142642-31-7

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142642-31-7 Usage

General Description

The chemical compound ((2,6-bis(1-methylethyl)phenoxy)sulfonyl)carbamic acid 2,6-bis(1-methylethyl)phenyl ester is an organic compound with the molecular formula C20H30NO6S. It is commonly used as a pesticide and herbicide. It is a white crystalline solid that is soluble in organic solvents but insoluble in water. This chemical is known for its ability to control a wide range of pests and weeds, making it a valuable tool in agriculture and pest control. However, it is important to handle and use this chemical carefully, as it can be toxic to humans and the environment if not used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 142642-31-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,6,4 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 142642-31:
(8*1)+(7*4)+(6*2)+(5*6)+(4*4)+(3*2)+(2*3)+(1*1)=107
107 % 10 = 7
So 142642-31-7 is a valid CAS Registry Number.
InChI:InChI=1/C25H35NO5S/c1-15(2)19-11-9-12-20(16(3)4)23(19)30-25(27)26-32(28,29)31-24-21(17(5)6)13-10-14-22(24)18(7)8/h9-18H,1-8H3,(H,26,27)

142642-31-7SDS

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 [2,6-di(propan-2-yl)phenyl] N-[2,6-di(propan-2-yl)phenoxy]sulfonylcarbamate

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:142642-31-7 SDS

142642-31-7Downstream Products

142642-31-7Relevant articles and documents

Inhibitors of acyl-CoA:Cholesterol O-acyltransferase. 17. Structure-activity relationships of several series of compounds derived from N-chlorosulfonyl isocyanate

Picard, Joseph A.,O'Brien, Patrick M.,Sliskovic, Drago R.,Anderson, Maureen K.,Bousley, Richard F.,Hamelehle, Katherine L.,Krause, Brian R.,Stanfield, Richard L.

, p. 1243 - 1252 (2007/10/03)

Several series of acyl-CoA:cholesterol O-acyltransferase inhibitors were prepared by the stepwise addition of nitrogen, oxygen, and sulfur nucleophiles to N-chlorosulfonyl isocyanate. The (aminosulfonyl)ureas 3-44 were the most potent inhibitors in vitro,

Oxysulfonyl carbamates

-

, (2008/06/13)

The present invention is directed to compounds of the following general Formula I, methods for using the compounds of Formula I, pharmaceutical compositions thereof, and processes for preparing the compounds. STR1 wherein X is oxygen or sulfur; wherein R

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