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2-(2-nitrophenyl)-3-p-tolylthiazolidin-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

388591-42-2

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388591-42-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 388591-42-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,8,5,9 and 1 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 388591-42:
(8*3)+(7*8)+(6*8)+(5*5)+(4*9)+(3*1)+(2*4)+(1*2)=202
202 % 10 = 2
So 388591-42-2 is a valid CAS Registry Number.

388591-42-2Downstream Products

388591-42-2Relevant academic research and scientific papers

One-pot synthesis of 1,3-thiazolidin-4-one using ammonium persulfate as catalyst

Ebrahimi, Sattar

, p. 587 - 592 (2016)

Ammonium persulfate can be used as a homogeneous catalyst for three-component one-pot synthesis of some 1,3-thiazolidin-4-one derivatives from aldehydes, amines and mercaptoacetic acid under solvent-free conditions with good yields. The characterization o

Ionic liquid immobilized on FeNi3 as catalysts for efficient, green, and one-pot synthesis of 1,3-thiazolidin-4-one

Sadeghzadeh, Seyed Mohsen,Daneshfar, Faeze

, p. 440 - 444 (2015/01/16)

A magnetically ionic liquid (ILs) supported on FeNi3 nanocatalyst was synthesized and evaluated as a recoverable catalyst for the synthesis of 1,3-thiazolidin-4-one. The main targets are solvent-free conditions, rapid (immediately) and easy immobilization technique, and low cost precursors for the preparation of highly active and stable MPs with high densities of functional groups. The inorganic, magnetic, solid base catalyst was characterized via Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), thermal gravimetric analysis (TGA), transmission electron microscopy (TEM) and vibrating sample magnetometer (VSM). The catalyst is active for the synthesis of 1,3-thiazolidin-4-ones and the products are isolated in high to excellent yields. Supporting this base catalyst on magnetic particles offers a simple and non-energy-intensive method for recovery and reuse of the catalyst by applying an external magnet. Isolated catalysts were reused for new rounds of reactions without significant loss of their catalytic activity.

One-pot synthesis of 1,3-thiazolidin-4-one using Bi(SCH2COOH) 3 as catalyst

Foroughifar, Naser,Ebrahimi, Sattar

, p. 389 - 391 (2013/07/19)

A catalytic multi-component reaction involving aromatic amine, aromatic aldehydes, mercapto acid as substrates and Bi(SCH2COOH)3 as catalyst under solvent free conditions, afforded thiazolidin-4-one in good yields. The efficiency of the catalyst was proved with a variety of substrates, ranging from electron-deficient to electron-rich aldehydes.

Ionic liquid mediated and promoted eco-friendly preparation of thiazolidinone and pyrimidine nucleoside-thiazolidinone hybrids and their antiparasitic activities

Zhang, Xinying,Li, Xiaoyan,Li, Dongfang,Qu, Guirong,Wang, Jianji,Loiseau, Philippe M.,Fan, Xuesen

scheme or table, p. 6280 - 6283 (2010/08/06)

Without any catalyst, 2,3-disubstituted-1,3-thiazolidin-4-one derivatives were synthesized efficiently via the three-component reaction of aldehyde, amine and mercaptoacetic acid in [bmim][PF6]. The whole procedure is simple and straightforward

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