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Propanedioic acid, [[(3-bromophenyl)amino]thioxomethyl]-, diethyl ester is a complex organic compound with the chemical formula C13H16BrNO4S. It is a derivative of propanedioic acid, featuring a 3-bromophenyl group attached to an aminothioxomethyl moiety. The molecule is further characterized by two ethyl ester groups, which are attached to the carboxylic acid groups of the propanedioic acid backbone. Propanedioic acid, [[(3-bromophenyl)amino]thioxomethyl]-, diethyl ester is likely to be used in the synthesis of pharmaceuticals or other organic compounds due to its unique structure and functional groups. It is important to handle Propanedioic acid, [[(3-bromophenyl)amino]thioxomethyl]-, diethyl ester with care, as it may have potential health and environmental impacts due to its bromine content and complex structure.

3288-18-4

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3288-18-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3288-18-4 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, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3288-18:
(6*3)+(5*2)+(4*8)+(3*8)+(2*1)+(1*8)=94
94 % 10 = 4
So 3288-18-4 is a valid CAS Registry Number.

3288-18-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 2-[(3-bromophenyl)carbamothioyl]propanedioate

1.2 Other means of identification

Product number -
Other names <3-Brom-phenylthiocarbamoyl>-malonsaeure-diaethylester

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:3288-18-4 SDS

3288-18-4Relevant academic research and scientific papers

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.

Synthesis of ethyl 2-arylaminoimidazo[2,1-b]benzothiazole-3-carboxylates

Khalafy, Jabbar,Ebrahimlo, Ali Reza Molla,Dilmaghani, Karim Akbari

, p. 1347 - 1352 (2007/10/03)

3-Arylamino-4-ethoxycarbonylisoxazol-5(2H)-ones, substituted on nitrogen with a benzothiazole group, reacts with triethylamine in ethanol under reflux conditions to provide a convenient synthesis of ethyl 2-arylaminoimidazo[2,1-b] benzothiazole-3-carboxyl

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