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N-(2-ethylphenyl)benzo[d]oxazol-2-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1268341-70-3

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1268341-70-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1268341-70-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,8,3,4 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1268341-70:
(9*1)+(8*2)+(7*6)+(6*8)+(5*3)+(4*4)+(3*1)+(2*7)+(1*0)=163
163 % 10 = 3
So 1268341-70-3 is a valid CAS Registry Number.

1268341-70-3Downstream Products

1268341-70-3Relevant academic research and scientific papers

Iodide catalyzed synthesis of 2-aminobenzoxazoles via oxidative cyclodesulfurization of phenolic thioureas with hydrogen peroxide

Yadav, Vinod K.,Srivastava, Vishnu P.,Yadav, Lal Dhar S.

, p. 252 - 255 (2017/12/26)

A convenient and efficient oxidative cyclodesulfurization of o-phenolic thioureas to 2-aminobenzoxazoles employing TBAI (tetrabutylammonium iodide)/H2O2 catalyst/reagent system is reported. The protocol utilizes and offers a number o

Visible-light-promoted cyclodesulfurization of phenolic thioureas: An organophotoredox catalytic approach to 2-aminobenzoxazoles

Yadav, Vinod K.,Srivastava, Vishnu P.,Yadav, Lal Dhar S.

, p. 155 - 158 (2015/12/24)

A facile and efficient one-pot operation for the photo-oxidative cyclodesulfurization of o-phenolic thioureas to afford 2-aminobenzoxazoles is reported. The protocol could be executed under visible light irradiation employing eosin Y as an organophotoredo

An economically and environmentally sustainable synthesis of 2-aminobenzothiazoles and 2-aminobenzoxazoles promoted by water

Zhang, Xinying,Jia, Xuefei,Wang, Jianji,Fan, Xuesen

supporting information; experimental part, p. 413 - 418 (2011/04/16)

Tandem reactions of isothiocyanates (1) with 2-aminothiophenols (2), or isothiocyanates (1) with 2-aminophenols (4), were carried out rapidly and efficiently in water. A significant rate acceleration of the reaction between 1a and 2a in water compared wit

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