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(Z)-5-tosyloxy-4-[2-(1',3'-benzodioxol-6'-bromo-5'-yl)]-1-ethenyl-2-bromopyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1114235-31-2

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1114235-31-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1114235-31-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,1,4,2,3 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1114235-31:
(9*1)+(8*1)+(7*1)+(6*4)+(5*2)+(4*3)+(3*5)+(2*3)+(1*1)=92
92 % 10 = 2
So 1114235-31-2 is a valid CAS Registry Number.

1114235-31-2Downstream Products

1114235-31-2Relevant academic research and scientific papers

A new approach to the benzopyridoxepine core by metal mediated intramolecular biaryl ether formation

Serban, Georgeta,Abe, Hitoshi,Takeuchi, Yasuo,Harayama, Takashi

experimental part, p. 2949 - 2958 (2009/05/31)

This paper presents a concise synthesis of the novel [1,3]dioxo[d]benzoxepino[2,3-c]-6-bromopyridine 1. The benzopyridoxepine core has been obtained by intramolecular coupling of a benzopyridylethene that is in turn obtained from the Wittig reaction. Thus, the synthesis was accomplished in a very good yield by implementation of an intramolecular palladium-catalyzed biaryl ether formation (Buchwald-Hartwig type reaction). An alternative approach based on the copper-mediated C-O bond formation (intramolecular Ullmann reaction) was not successful.

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