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2-(2,3-dichlorophenyl)-benzothiazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

902096-86-0

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902096-86-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 902096-86-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,2,0,9 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 902096-86:
(8*9)+(7*0)+(6*2)+(5*0)+(4*9)+(3*6)+(2*8)+(1*6)=160
160 % 10 = 0
So 902096-86-0 is a valid CAS Registry Number.

902096-86-0Downstream Products

902096-86-0Relevant academic research and scientific papers

A simple approach to benzothiazoles from 2-chloronitrobenzene, elemental sulfur, and aliphatic amine under solvent-free and catalyst-free conditions

Tong, Yao,Pan, Qiang,Jiang, Zengqiang,Miao, Dazhuang,Shi, Xuesong,Han, Shiqing

, p. 5499 - 5503 (2014)

A novel solvent-free and catalyst-free synthesis of benzothiazoles from 2-chloronitrobenzene, elemental sulfur, and aliphatic amine has been developed. The reaction tolerated a wide range of functionalities, and various benzothiazoles were synthesized in moderate to good yields in the absence of external oxidant or reductant.

Aerobic oxidative synthesis of quinazolinones and benzothiazoles in the presence of laccase/DDQ as a bioinspired cooperative catalytic system under mild conditions

Abdelrasoul, Amira,Ghorashi, Nadia,Moradi, Reza,Rostami, Amin,Shokri, Zahra

, p. 14254 - 14261 (2020/04/23)

The current study applied laccase/DDQ as a bioinspired cooperative catalytic system for the synthesis of quinazolinones (80-95% yield) and benzothiazoles (65-98% yield) using air or O2 as ideal oxidants in aqueous media at ambient temperature. The aerobic oxidative cyclization reactions occur in two steps: (i) chemical cyclization; (ii) chemoenzymatic oxidation. These methods are more environment-friendly, efficient, simple and practical than other reported methods due to the use of O2 as an oxidant, laccase as an eco-friendly biocatalyst, aqueous media as the solvent and free from any toxic transition metal and halide catalysts. Therefore, these methods can be applied in pharmaceutical and other sensitive synthetic procedures.

Catalyst-Free Synthesis of 2-Arylbenzothiazoles in an Air/DMSO Oxidant System

Hu, Renhe,Li, Xiaotong,Tong, Yao,Miao, Dazhuang,Pan, Qiang,Jiang, Zengqiang,Gan, Haifeng,Han, Shiqing

supporting information, p. 1387 - 1390 (2016/05/24)

A straightforward strategy for the synthesis of 2-arylbenzothiazoles from 2-aminothiophenol and aryl aldehydes in air/DMSO oxidant system has been developed. This reaction is operationally simple, proceeds without catalysts, tolerates a wide range of func

Facile one-pot synthesis of 2-arylbenzothiazoles catalyzed by H3PO4/TiO2-ZrO2(1/1) under solvent-free conditions

Naeimi, Hossein,Heidarnezhad, Arash

supporting information, p. 594 - 603 (2016/06/06)

A highly efficient and simple protocol for the preparation of 2-arylbenzothiazoles through condensation of 2-aminothiophenol and different aldehydes in the presence of H3PO4/TiO2-ZrO2(1/1)-cetyl pyridinium bromi

Titanium Tetrabutoxide (TTBO) as Efficient Catalyst for Rapid One Pot Synthesis of 2-Arylbenzothiazoles under Mild Conditions

Naeimi, Hossein,Heidarnezhad, Arash

, p. 1004 - 1008 (2016/02/18)

An effective strategy has been developed for rapid and efficient one pot synthesis of 2-arylbenzothiazoles from readily available 2-aminothiophenol and aromatic aldehydes catalyzed by TTBO in high yields and short reaction times. This strategy allows acce

Synthesis of 2-arylbenzothiazoles using nano BF3/SiO2 as a reusable and efficient heterogeneous catalyst under mild conditions

Naeimi, Hossein,Heidarnezhad, Arash

, p. 493 - 501 (2014/08/18)

2-Arylbenzothiazoles were synthesized via condensation of 2-aminothiophenol and different aldehydes catalyzed by nano silica-supported boron trifluoride (nano BF3/SiO2) as an efficient and reusable catalyst in high yields and short r

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