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Methyl 2-propyl-1,3-benzoxazole-6-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

330206-41-2

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330206-41-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 330206-41-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,0,2,0 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 330206-41:
(8*3)+(7*3)+(6*0)+(5*2)+(4*0)+(3*6)+(2*4)+(1*1)=82
82 % 10 = 2
So 330206-41-2 is a valid CAS Registry Number.

330206-41-2Downstream Products

330206-41-2Relevant academic research and scientific papers

Poly (ethylene glycol)-bound sulphonic acid as a novel catalyst for synthesis of benzoxazoles

Chikhale, Rupesh V.,Pant, Amit M.,Menghani, Sunil S.,Wadibhasme, Pankaj G.,Khedekar, Pramod B.

, p. 254 - 262 (2013/12/04)

ABSTRACT Ahighly efficient, simple and rapid method for the preparation of various 2-aminobenzoxazoles and other benzoxazole derivatives using a catalytic amount of poly (ethylene glycol)-bound sulphonic acid (PEG-SO3H) is described. PEG-SO3H is found to be economical and reusable catalyst with low catalytic loading. The percentage yield was found to be satisfactory, experimental set-up and purification of final products is facile and easy. GRAPHICAL ABSTRACT.

Extending the scope of chromium - Manganese redox-coupled reactions: A one-pot synthesis of benzoxazoles

Hari,Karan,Rodrigues,Miller

, p. 991 - 996 (2007/10/03)

A critically important strategy for synthetic chemistry is the development of domino processes: those capable of concatenating multiple transformations into a single step. Such transformations not only provide an increase in synthetic efficiency, but also imply the development of a significant degree of mechanistic understanding. We report herein a new domino reaction, in which a chromium-manganese redox couple is employed both to catalytically reduce an o-hydroxy nitroarene and to oxidatively cyclize a subsequently formed imine. We find that the reaction is most effective for starting o-hydroxy nitroarenes with a strongly electron-withdrawing group at the para position.

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