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3-(benzo[d]thiazol-2-yl)-2-(4-bromophenyl)thiazolidin-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70048-70-3

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70048-70-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70048-70-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,0,4 and 8 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 70048-70:
(7*7)+(6*0)+(5*0)+(4*4)+(3*8)+(2*7)+(1*0)=103
103 % 10 = 3
So 70048-70-3 is a valid CAS Registry Number.

70048-70-3Downstream Products

70048-70-3Relevant academic research and scientific papers

Design of a new multi-functional catalytic system Ni/SO3H?zeolite-Y for three-component synthesis of: N -benzo-imidazo- or -thiazole-1,3-thiazolidinones

Banibairami, Soodabeh,Kalhor, Mehdi

, p. 41410 - 41423 (2020/11/30)

In this investigation, a nanoporous zeolite-NaY supported sulfonic acid was synthesized and Ni(ii) ions were successfully stabilized on SO3H?zeolite-Y (Ni/SO3H?zeolite-Y). This novel type of zeolitic nanocomposite was characterized using various techniques including FT-IR, FE-SEM, TGA, BET and EDX. Ni/SO3H?zeolite-Y was used as a multi-functional and highly active nanocatalyst for the three-component synthesis of 3-benzimidazolyl-1,3-thiazolidin-4-ones and new 3-benzthiazoleyl-1,3-thiazolidin-4-ones via cyclocondensation of 2-aminobenzimidazole or 2-aminobenzothiazole, aromatic aldehydes and thioglycolic acid in acetone-H2O at room temperature. This economical chemical procedure has advantages such as excellent yield in short reaction times, convenient manipulation and high purity of products, applicability to a broad range of substrates, and the use of a nontoxic and heterogeneous acid catalyst with good reusability.

Synthesis and biological significance of 2-aminobenzothiazole derivatives

Srivastava,Shukla

experimental part, p. 306 - 309 (2009/05/31)

Several new 2-N-(substituted benzyledine)-imino-1,3-benzothiazole 1; 2-[2′-(substituted phenyl)-4′-oxo-1′,3′-thiazolidine]-1, 3-benzothiazole 2 and 2-[5′-(arylidene)-2′-substituted phenyl-4′-oxo-1′,3′-thiazolidine]-1,3-benzothiazole 3 have been synthesize

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