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Diethyl N-(2-methylphenyl)thiocarbamoylmalonate is a chemical compound with the molecular formula C16H19NO3S. It is an organic compound that belongs to the class of thiocarbamates, which are derivatives of carbamic acid. This specific compound features a 2-methylphenyl group attached to a thiocarbamoylmalonate moiety, which consists of a thiocarbonyl group (C=S) bonded to a carbamoyl group (CONH2) and a malonate ester (C4H6O4). The compound is characterized by its potential use as a pesticide or herbicide, and it is known for its ability to inhibit certain plant growth processes. It is typically synthesized through the reaction of diethyl malonate with 2-methylaniline and carbon disulfide in the presence of a base. Due to its chemical structure and properties, diethyl N-(2-methylphenyl)thiocarbamoylmalonate is an important compound in the field of agrochemicals, where it may be used to control unwanted plant species in agricultural settings.

3288-01-5

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3288-01-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3288-01-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,8 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3288-01:
(6*3)+(5*2)+(4*8)+(3*8)+(2*0)+(1*1)=85
85 % 10 = 5
So 3288-01-5 is a valid CAS Registry Number.

3288-01-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl N-(2-methylphenyl)thiocarbamoylmalonate

1.2 Other means of identification

Product number -
Other names [2-Methyl-phenylthiocarbamoyl]-malonsaeure-diethylester

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:3288-01-5 SDS

3288-01-5Relevant academic research and scientific papers

Synthesis and crystal structure of ethyl 2-(benzo[d]oxazol-2-yl)-5-oxo-3- (o-tolylamino)-2,5-dihydroisoxazole-4-carboxylate

Poursattar Marjani,Khalafy,Noroozi Pesyan

, p. 27 - 31 (2013/08/24)

The titlecompoundethyl 2-(benzo[d]oxazol-2-yl)-5-oxo-3-(o-tolylamino)-2,5- dihydroisoxazole-4-carboxylate (5) was synthesized and studied by the single crystal X-ray diffraction method. Its structure was confirmed by IR, 1H and 13C N

Rearrangements of 2-pyridyl-3-arylaminoisoxazol-5(2H)-ones to imidazo[1,2-a]pyridines under flash-vacuum-pyrolysis

Setamdideh, Davood,Khanahmadzadeh, Salah,Khorshidi, Nasrin

experimental part, p. 2884 - 2890 (2012/07/17)

2-Pyridyl-3-arylaminoisoxazol-5(2H)-ones, rearranged under flash-vacuum-pyrolysis (FVP) conditions accompanied by elimination of carbon dioxide to give imidazo[1,2-a]pyridines in high to excellent yields (85-95 %).

Ethyl 5-oxo-3-arylamino-2,5-dihydroisoxazole-4-carboxylates as sources of imidazopyrimidine and aminoindole derivatives

Poursattar Marjani, Ahmad,Khalafy, Jabbar

body text, p. 847 - 858 (2011/08/21)

The reaction of ethyl 5-oxo-3-arylamino-2,5-dihydroisoxazole-4-carboxylates with 2-chloropyrimidine and 2-chlorobenzoxazole gave the corresponding isoxazolones with pyrimidine and benzoxazole rings substituted on N-2. Their rearrangements with triethylamine in ethanol produced the corresponding imidazopyrimidine and aminoindole derivatives, respectively, through intramolecular cyclisation. TUeBITAK.

Base-induced rearrangements of N-substituted 3-arylamino-isoxazol-5(2H)- ones to 2-aryl-aminoimidazo[1,2-a]pyridines

Baradarani,Khalafy,Khadivi,Poursattar Marjani

, p. 594 - 599 (2013/07/11)

New N-substituted derivatives of 2-substituted 3-phenylamino- and 3-(1-naphthyl)aminoisoxazol-5(2H)-ones were synthesized. The reaction of isoxazolones with 2-chloro-5-nitropyridine gave the corresponding isoxazolones with a nitropyridyl group substituted

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