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N-(4-methylthiazol-2-yl)benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

37529-67-2

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37529-67-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37529-67-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,5,2 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 37529-67:
(7*3)+(6*7)+(5*5)+(4*2)+(3*9)+(2*6)+(1*7)=142
142 % 10 = 2
So 37529-67-2 is a valid CAS Registry Number.

37529-67-2Relevant academic research and scientific papers

N-(thiazol-2-yl)benzamide derivatives as a new series of supramolecular gelators: Role of methyl functionality and S?O interaction

Yadav, Priyanka,Ballabh, Amar

, (2020)

A new series of N-(thiazol-2-yl) benzamide derivatives were synthesized, characterized and investigated for their gelation behavior with the aim to elucidate the role of methyl functionality and multiple non-covalent interactions on gelation/non-gelation

Modification and biological evaluation of thiazole derivatives as novel inhibitors of metastatic cancer cell migration and invasion

Zheng, Shilong,Zhong, Qiu,Xi, Yulan,Mottamal, Madhusoodanan,Zhang, Qiang,Schroeder, Richard L.,Sridhar, Jayalakshmi,He, Ling,McFerrin, Harris,Wang, Guangdi

, p. 6653 - 6667 (2014/10/15)

Fascin has recently emerged as a potential therapeutic target, as its expression in cancer cells is closely associated with tumor progression and metastasis. Following the initial discovery of a series of thiazole derivatives that demonstrated potent anti

Design and synthesis of noncompetitive metabotropic glutamate receptor subtype 5 antagonists

Kulkarni, Santosh S.,Nightingale, Barbara,Dersch, Christina M.,Rothman, Richard B.,Newman, Amy Hauck

, p. 3371 - 3375 (2007/10/03)

A series of diaryl amides was designed and synthesized as novel nonethynyl mGluR5 antagonists. The systematic variation of the pharmacophoric groups led to the identification of a lead compound that demonstrated micromolar affinity for the mGluR5. Further optimization resulted in compounds with improved binding affinities and antagonist profiles, in vitro.

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