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4-[(2-bromobenzyl)oxy]-1,6-dimethyl-1,2-dihydropyridin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1033480-95-3

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1033480-95-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1033480-95-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,3,4,8 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1033480-95:
(9*1)+(8*0)+(7*3)+(6*3)+(5*4)+(4*8)+(3*0)+(2*9)+(1*5)=123
123 % 10 = 3
So 1033480-95-3 is a valid CAS Registry Number.

1033480-95-3Relevant academic research and scientific papers

Pd-catalysed intramolecular regioselective arylation of 2-pyrones, pyridones, coumarins and quinolones by C–H bond functionalization

Nolan, Marie-Therese,Bray, Joshua T.W.,Eccles, Kevin,Cheung, Man Sing,Lin, Zhenyang,Lawrence, Simon E.,Whitwood, Adrian C.,Fairlamb, Ian J.S.,McGlacken, Gerard P.

, p. 7120 - 7127 (2014)

The intramolecular arylation of 2-pyrones, 2-pyridones, coumarins and quinolones is reported using PdII precatalyst sources without added phosphine ligands. The excellent yields and convenient reagents enables the formation of various analogues

Pd/pivalic acid mediated direct arylation of 2-pyrones and related heterocycles

Pardo, Leticia M.,Prendergast, Aisling M.,Nolan, Marie-T.,Muimhneachin, Eoin,McGlacken, Gerard P.

, p. 3540 - 3550 (2015/06/08)

Abstract Direct arylation represents a favourable alternative to traditional cross-coupling reactions and has found widespread use with simple aryls and robust heterocycles. Herein a direct arylation protocol has been optimised and applied to more delicat

Intramolecular cyclization reaction - Palladium(0)-catalyzed cyclization is more effective than tin hydride mediated reaction

Majumdar, Krishna C.,Debnath, Pradip,Taher, Abu,Pal, Amarta K.

, p. 325 - 332 (2008/09/20)

Intramolecular CH arylation of pyrone, pyridone, uracil, imidazole, and benzimidazole derivatives are carried out in the presence of a Pd catalyst to form potentially bioactive fused heterocyclic compounds, whereas the n-Bu 3SnH-mediated aryl radical cyclization of the precursors 3 afforded mainly halogen-reduced uncyclized products.

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