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N-(1,3-benzothiazol-2-yl)-2-naphthamide is a chemical compound with the molecular formula C18H11N3OS. It is a derivative of naphthamide, featuring a benzothiazole group attached to the nitrogen atom. N-(1,3-benzothiazol-2-yl)-2-naphthamide is known for its potential applications in the field of organic chemistry, particularly as a building block for the synthesis of more complex molecules. It may also be of interest in materials science due to its unique structure, which could contribute to specific properties in various applications. The compound's structure and properties make it a subject of study for researchers looking to understand and develop new chemical entities with tailored characteristics.

5690-02-8

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5690-02-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5690-02-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,9 and 0 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5690-02:
(6*5)+(5*6)+(4*9)+(3*0)+(2*0)+(1*2)=98
98 % 10 = 8
So 5690-02-8 is a valid CAS Registry Number.

5690-02-8Downstream Products

5690-02-8Relevant academic research and scientific papers

Access to Amide from Aldimine via Aerobic Oxidative Carbene Catalysis and LiCl as Cooperative Lewis Acid

Wang, Guanjie,Fu, Zhenqian,Huang, Wei

supporting information, p. 3362 - 3365 (2017/07/13)

Herein, an efficient route to amides from aldimines via aza-Breslow intermediates through aerobic oxidative carbene catalysis with LiCl as a cooperative Lewis acid is described. Many of the obtained N-heteroarylamides feature biological activity. Ambient

Facile synthesis of N-acyl 2-aminobenzothiazoles by NHC-catalyzed direct oxidative amidation of aldehydes

Premaletha, Sethulekshmy,Ghosh, Arghya,Joseph, Sumi,Yetra, Santhivardhana Reddy,Biju, Akkattu T.

supporting information, p. 1478 - 1481 (2017/02/05)

A mild, general, and high yielding synthesis of N-acyl 2-aminobenzothiazoles has been demonstrated by N-heterocyclic carbene (NHC)-organocatalyzed direct amidation of aldehydes with 2-aminobenzothiazoles proceeding via acyl azolium intermediates. The carbene generated from the triazolium salt under oxidative conditions was the key for the success of this reaction. The method was subsequently applied to the synthesis of various biologically important N-acyl 2-aminobenzothiazoles.

IMIDE-CONTAINING BENZOTHIAZOLE DERIVATIVE OR ITS SALT AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME

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Paragraph 118; 119; 120, (2013/04/10)

The present invention provides an imide-containing benzothiazole derivative or its pharmaceutically acceptable salt, a process for the preparation thereof, and a pharmaceutical composition comprising the same. The imide-containing benzothiazole derivative or its pharmaceutically acceptable salt can selectively inhibit the protein-protein interaction between KRS and a laminin receptor (LR), thereby inhibiting migration of cancer cells. Therefore, the imide-containing benzothiazole derivative or its pharmaceutically acceptable salt may be usefully applied for preventing or treating the diseases associated with cancer cell metastasis.

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