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5-Benzyloxy-2-(2,5-diMethylpyrrol-1-yl)pyridine is a complex chemical compound characterized by a benzene ring connected to an oxygen atom, which is further linked to a pyridine ring. This pyridine ring features a methylpyrrol group at the 2-position and a methyl group at the 5-position. Its unique molecular structure and properties make it a promising candidate for various applications in organic synthesis, medicinal chemistry, and material science.

1083329-33-2

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1083329-33-2 Usage

Uses

Used in Organic Synthesis:
5-Benzyloxy-2-(2,5-diMethylpyrrol-1-yl)pyridine is used as a building block for the synthesis of various biologically active molecules and functional materials. Its unique structure allows for the creation of new compounds with potential applications in various fields.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 5-Benzyloxy-2-(2,5-diMethylpyrrol-1-yl)pyridine is used as a potential candidate for drug discovery and design. Its structural features suggest that it may exhibit pharmacological activity, which could be harnessed for therapeutic purposes.
Used in Material Science:
5-Benzyloxy-2-(2,5-diMethylpyrrol-1-yl)pyridine is also utilized in material science for the development of new functional materials. Its properties may contribute to the creation of advanced materials with specific characteristics, such as improved stability or reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 1083329-33-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,3,3,2 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1083329-33:
(9*1)+(8*0)+(7*8)+(6*3)+(5*3)+(4*2)+(3*9)+(2*3)+(1*3)=142
142 % 10 = 2
So 1083329-33-2 is a valid CAS Registry Number.

1083329-33-2Downstream Products

1083329-33-2Relevant academic research and scientific papers

Pyridine and pyrimidine analogs of acetaminophen as inhibitors of lipid peroxidation and cyclooxygenase and lipoxygenase catalysis

Nam, Tae-Gyu,Nara, Susheel J.,Zagol-Ikapitte, Irene,Cooper, Thomas,Valgimigli, Luca,Oates, John A.,Porter, Ned A.,Boutaud, Olivier,Pratt, Derek A.

scheme or table, p. 5103 - 5112 (2010/04/04)

Herein we report an investigation of the efficacy of pyridine and pyrimidine analogs of acetaminophen (ApAP) as peroxyl radical-trapping antioxidants and inhibitors of enzyme-catalyzed lipid peroxidation by cyclooxygenases (COX) and lipoxygenases (LOX). I

A simple Cu-catalyzed coupling approach to substituted 3-pyridinol and 5-pyrimidinol antioxidants

Nara, Susheel J.,Jha, Mukund,Brinkhorst, Johan,Zemanek, Tony J.,Pratt, Derek A.

experimental part, p. 9326 - 9333 (2009/04/06)

(Chemical Equation Presented) A convenient approach to 3-pyridinols and 5-pyrimidinols via a two-step Cu-catalyzed benzyloxylation/catalytic hydrogenation sequence is presented. The corresponding 3-pyridinamines and 5-pyrimidinamines can be prepared in an analogous sequence utilizing benzylamine in lieu of benzyl alcohol. The radical-scavenging ability of these derivatives are preliminarily explored and reveal that the increased acidities of the pyridinols and pyrimidinols render them susceptible to more significant kinetic solvent effects when compared to phenols.

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