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3-Benzyloxy-5-bromo-1-methyl-1H-pyridin-2-one is a chemical compound with the molecular formula C13H10BrNO2. It is a derivative of pyridin-2-one and contains a bromine atom, a methyl group, and a benzyloxy group attached to the pyridin-2-one ring. 3-Benzyloxy-5-broMo-1-Methyl-1H-pyridin-2-one is commonly used in organic synthesis and pharmaceutical research due to its potential biological and pharmacological activities. Its structure and properties make it a valuable building block in the development of new drugs and biologically active compounds. Additionally, its functional groups allow for further modification and derivatization to create new chemical entities with diverse biological activities.

1333146-86-3

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1333146-86-3 Usage

Uses

Used in Organic Synthesis:
3-Benzyloxy-5-bromo-1-methyl-1H-pyridin-2-one is used as a building block in organic synthesis for the creation of new chemical entities with diverse biological activities. Its functional groups enable further modification and derivatization, making it a valuable component in the development of novel compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 3-Benzyloxy-5-bromo-1-methyl-1H-pyridin-2-one is used as a starting material for the development of new drugs and biologically active compounds. Its potential biological and pharmacological activities make it a promising candidate for various therapeutic applications, including the treatment of diseases and disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 1333146-86-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,3,1,4 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1333146-86:
(9*1)+(8*3)+(7*3)+(6*3)+(5*1)+(4*4)+(3*6)+(2*8)+(1*6)=133
133 % 10 = 3
So 1333146-86-3 is a valid CAS Registry Number.

1333146-86-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-benzyloxy-5-bromo-1-methyl-1H-pyridin-2-one

1.2 Other means of identification

Product number -
Other names 3-(Benzyloxy)-5-bromo-1-methylpyridin-2(1H)-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1333146-86-3 SDS

1333146-86-3Relevant academic research and scientific papers

New Pyridinones and Isoquinolinones as Inhibitors of the Bromodomain BRD9

-

, (2018/03/25)

The present invention encompasses compounds of general formula (I) wherein the groups R1 to R9, X1 and X2 have the meanings given in the claims and in the specification. The compounds of the invention are suitable for the treatment of diseases characterized by excessive or abnormal cell proliferation, e.g. cancer, pharmaceutical preparations containing such compounds and their uses as a medicament.

Catechols and 3-hydroxypyridones as inhibitors of the DNA repair complex ERCC1-XPF

Chapman, Timothy M.,Gillen, Kevin J.,Wallace, Claire,Lee, Maximillian T.,Bakrania, Preeti,Khurana, Puneet,Coombs, Peter J.,Stennett, Laura,Fox, Simon,Bureau, Emilie A.,Brownlees, Janet,Melton, David W.,Saxty, Barbara

, p. 4097 - 4103 (2015/11/03)

Catechol-based inhibitors of ERCC1-XPF endonuclease activity were identified from a high-throughput screen. Exploration of the structure-activity relationships within this series yielded compound 13, which displayed an ERCC1-XPF IC50 of 0.6 μM, high selectivity against FEN-1 and DNase I and activity in nucleotide excision repair, cisplatin enhancement and γH2AX assays in A375 melanoma cells. Screening of fragments as potential alternatives to the catechol group revealed that 3-hydroxypyridones are able to inhibit ERCC1-XPF with high ligand efficiency, and elaboration of the hit gave compounds 36 and 37 which showed promising ERCC1-XPF IC50 values of 10 μM.

INHIBITORS OF CATECHOL O-METHYL TRANSFERASE AND THEIR USE IN THE TREATMENT OF PSYCHOTIC DISORDERS

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, (2011/10/03)

The present invention relates to 4-pyridinone compounds which are inhibitors of catechol O-methyltransferase (COMT), and are useful in the treatment and prevention of neurological and psychiatric disorders and diseases in which COMT enzyme is involved. Th

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