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(4-amino-2-p-tolylamino-thiazol-5-yl)-phenyl-methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

107401-68-3

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107401-68-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107401-68-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,4,0 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 107401-68:
(8*1)+(7*0)+(6*7)+(5*4)+(4*0)+(3*1)+(2*6)+(1*8)=93
93 % 10 = 3
So 107401-68-3 is a valid CAS Registry Number.

107401-68-3Downstream Products

107401-68-3Relevant academic research and scientific papers

One-pot sequential multicomponent route to 2,4-diaminothiazoles - A facile approach to bioactive agents for cancer therapeutics

Sreejalekshmi, Kumaran G.,Rajasekharan, Kallikat N.

, p. 3627 - 3629 (2012)

A facile one-pot sequential three-component route to 2,4-diaminothiazoles is reported. The new approach employs the mildest reaction conditions and commercially available reagents to generate diverse 2-alkyl/arylamino-4-amino-5- aroyl/heteroylthiazoles in short reaction times, good yield, and purity.

An efficient protocol for solid phase aminothiazole synthesis

Sreejalekshmi, Kumaran G.,Devi, Satyabhama K.C.,Rajasekharan, Kallikat N.

, p. 6179 - 6182 (2006)

An efficient synthesis of 2,4-diamino-5-ketothiazoles under solid phase conditions has been achieved by the reaction of polymer supported amidinothioureas with α-haloketones. This novel synthetic approach involving traceless cleavage from the support is s

DIAMINOTHIAZOLE COMPOUNDS, COMPOSITIONS AND METHODS OF USE

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Paragraph 00163; 00164; 00165; 00184, (2018/05/27)

The disclosure relates to diaminothiazole derivatives of formula (I) where the variables are as defined herein, pharmaceutical compositions containing such compounds, and methods for the use of such compounds and compositions for the treatment of hyperpro

2-Arylamino-4-amino-5-aroylthiazoles. "One-pot" synthesis and biological evaluation of a new class of inhibitors of tubulin polymerization

Romagnoli, Romeo,Baraldi, Pier Giovanni,Carrion, Maria Dora,Cruz-Lopez, Olga,Cara, Carlota Lopez,Basso, Giuseppe,Viola, Giampietro,Khedr, Mohammed,Balzarini, Jan,Mahboobi, Siavosh,Sellmer, Andreas,Brancale, Andrea,Hamel, Ernest

supporting information; experimental part, p. 5551 - 5555 (2010/02/28)

The essential role of microtubules in mitosis makes them a major target of compounds useful for cancer therapy. In our search for potent antitumor agents, a novel series of 2-anilino-4-amino-5-aroylthiazoles was synthesized and evaluated for antiprolifera

Studies on the Synthesis of 5-Acyl-2,4-diaminothiazoles from Amidinothioureas

Rajasekharan, K. N.,Nair, K. P.,Jenardanan, G. C.

, p. 353 - 355 (2007/10/02)

1-Alkyl or aryl-3-amidinothioureas with or without substituents on the amidino moiety react with α-haloketones to yield 5-acyl-2,4-diaminothiazoles.

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