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Thiocyanic acid, 2,6-dimethyl-4-[[(methylamino)carbonyl]oxy]phenyl ester, also known as Fenpyroximate, is a chemical compound with the molecular formula C11H12N2O3S. It is a member of the pyrrole carboxamide family and is primarily used as an insecticide. Fenpyroximate works by inhibiting the electron transport system in the mitochondria of insects, leading to their paralysis and eventual death. It is effective against a wide range of pests, including aphids, whiteflies, and spider mites, and is known for its selective action and low mammalian toxicity. The compound is used in agriculture to protect crops from damage caused by these pests, contributing to more efficient and sustainable farming practices.

6074-44-8

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6074-44-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6074-44-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,7 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6074-44:
(6*6)+(5*0)+(4*7)+(3*4)+(2*4)+(1*4)=88
88 % 10 = 8
So 6074-44-8 is a valid CAS Registry Number.

6074-44-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl-carbamic acid 3,5-dimethyl-4-thiocyanato-phenyl ester

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

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More Details:6074-44-8 SDS

6074-44-8Downstream Products

6074-44-8Relevant academic research and scientific papers

Straightforward Access to Thiocyanates via Dealkylative Cyanation of Sulfoxides

Todorovi?, Uro?,Klose, Immo,Maulide, Nuno

supporting information, p. 2510 - 2513 (2021/04/13)

Thiocyanates, versatile building blocks in organic synthesis, are shown to be easily accessible via an interrupted Pummerer reaction of sulfoxides. This facile dealkylative functionalization proceeds under mild conditions through electrophilic activation of the sulfoxide partner. The resulting thiocyanate itself can serve as a handle for diversification in a straightforward one-pot procedure.

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