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Carbamothioic acid, diethyl-, S-(3-methylphenyl) ester, also known as fenpropathrin, is a synthetic pyrethroid insecticide used to control a wide range of pests in agriculture, horticulture, and public health. It is a colorless to pale yellow liquid with a chemical formula of C19H22N2O4S. Fenpropathrin acts as a neurotoxin, targeting the nervous system of insects by prolonging the opening of sodium channels, leading to paralysis and eventual death. It is effective against various insects, including mosquitoes, flies, and aphids, and is known for its rapid knockdown effect and low mammalian toxicity. However, due to its potential environmental impact and concerns over resistance development in pests, its use is regulated in many countries.

6399-00-4

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6399-00-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6399-00-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,9 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6399-00:
(6*6)+(5*3)+(4*9)+(3*9)+(2*0)+(1*0)=114
114 % 10 = 4
So 6399-00-4 is a valid CAS Registry Number.

6399-00-4SDS

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 S-(3-methylphenyl)-N,N-diethylcarbamate

1.2 Other means of identification

Product number -
Other names S-[m-Tolyl]-N,N-diethyl-thiolcarbamat

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:6399-00-4 SDS

6399-00-4Relevant academic research and scientific papers

A facile method for the synthesis of thiocarbamates: Palladium-catalyzed reaction of disulfide, amine, and carbon monoxide

Nishiyama, Yutaka,Kawamatsu, Hiroaki,Sonoda, Noboru

, p. 2551 - 2554 (2007/10/03)

(Equation Presented) A new method for the synthesis of thiocarbamates has been developed. When dialkyl or diaryl disulfides were allowed to react with secondary amines and carbon monoxide in the presence of a catalytic amount of a palladium complex, the thiocarbamates were obtained in moderate to good yields. In contrast to that of secondary amines, in the reaction of a primary amine, no formation of thiocarbamate was confirmed, but urea was formed in good yield.

Conversion of sterically hindered phenols into the corresponding N,N-dimethylarenesulfonamides via the Newman-Kwart rearrangement

Wagenaar, Anno,Engberts, Jan B. F. N.

, p. 91 - 94 (2007/10/02)

The 2-alkyl- and 2,6-dialkylbenzenesulfonyl chlorides 5a-f were obtained in high yield by chlorination of the correspondingly substituted S-aryl N,N-dialkylthiocarbamates 4a-g.These precursors have been synthesized via the Newman-Kwart rearrangement of th

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