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2-(3-Methoxy-phenyl)-benzo[d]imidazo[2,1-b]thiazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79889-64-8

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79889-64-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79889-64-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,8,8 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 79889-64:
(7*7)+(6*9)+(5*8)+(4*8)+(3*9)+(2*6)+(1*4)=218
218 % 10 = 8
So 79889-64-8 is a valid CAS Registry Number.

79889-64-8Downstream Products

79889-64-8Relevant academic research and scientific papers

Synthesis of bridgehead nitrogen heterocycles on a solid surface

Ponnala, Shashikanth,Kumar, S. T. V. S. Kiran,Bhat, Bashir A.,Sahu, Devi Prasad

, p. 901 - 906 (2005)

Bridgehead nitrogen heterocycles were synthesized from heteroaromatic amidines and cyclic or acyclic α-bromoketones under solvent-free conditions at room temperature on a solid surface in excellent yields, which are higher than those obtained with hithert

Iron-catalyzed unprecedented formation of benzo[d]imidazo[2,1-b]thiazoles under solvent-free conditions

Balwe, Sandip Gangadhar,Jeong, Yeon Tae

, p. 107225 - 107232 (2016/11/28)

The unprecedented formation of benzo[d]imidazo[2,1-b]thiazole during iron-catalyzed coupling of 2-aminobenzothiazole, aldehydes with nitroalkane in air has been observed. This unique transformation possibly occurs through a sequential aza-Henry reaction and subsequent intramolecular cyclization, followed by denitration. A variety of substituted benzo[d]imidazo[2,1-b]thiazole are obtained using this protocol.

Imidazobenzothiazoles. 2. New Immunosuppressive Agents

Mase, Toshiyasu,Arima, Hideki,Tomioka, Kenichi,Yamada, Toshimitsu,Murase, Kiyoshi

, p. 386 - 394 (2007/10/02)

A series of 2-phenylimidazobenzothiazole derivatives was prepared and tested for immunological activities.Some of the compounds showed significant suppressive activity of delayed type hypersensitivity (DTH) without inhibition of humoral immunity in mice by oral administration.The most active compound was 2-(m-hydroxyphenyl)imidazobenzothiazole (20).

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