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Propanedioic acid, [[(3-methylphenyl)amino]thioxomethyl]-, diethyl ester, also known as 3-Methyl-N-(2-carbethoxyethyl)thiobenzamide, is a complex organic compound with the chemical formula C14H19NO3S. It is a derivative of propanoic acid, featuring a 3-methylphenyl group attached to an aminothioxomethyl moiety, and diethyl ester groups at both ends. Propanedioic acid, [[(3-methylphenyl)amino]thioxomethyl]-, diethyl ester is characterized by its unique structure, which includes a thioamide linkage and an ester functional group. It is typically synthesized for use in chemical research and as an intermediate in the preparation of various pharmaceuticals and agrochemicals. Due to its specific functional groups and structural features, it may exhibit reactivity with nucleophiles and electrophiles, making it a versatile building block in organic synthesis.

3288-02-6

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3288-02-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3288-02-6 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 3288-02:
(6*3)+(5*2)+(4*8)+(3*8)+(2*0)+(1*2)=86
86 % 10 = 6
So 3288-02-6 is a valid CAS Registry Number.

3288-02-6Relevant academic research and scientific papers

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

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

, p. 1347 - 1352 (2004)

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

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 %).

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