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Ethanone, 1-(2-amino-4-pyrimidinyl)-2-bromo(9CI) is a chemical compound belonging to the class of organic compounds known as pyrimidinones. These compounds are characterized by the presence of a pyrimidine ring, a six-member aromatic heterocycle, conjugated with a ketone. In this specific compound, the inclusion of a bromine atom and an amino group significantly alters its chemical properties. However, comprehensive information regarding its applications, toxicological profile, safety measures, and physical and chemical properties is currently limited and not extensively available in the public domain. Further research and studies are necessary to gain a deeper understanding of its potential uses and implications.

106157-91-9

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106157-91-9 Usage

Uses

Due to the limited information available on Ethanone, 1-(2-amino-4-pyrimidinyl)-2-bromo(9CI), it is challenging to provide a detailed list of its applications. However, based on its classification as a pyrimidinone, it can be inferred that Ethanone, 1-(2-amino-4-pyrimidinyl)-2-bromo- (9CI) may have potential applications in various fields, such as pharmaceuticals, materials science, or chemical research. Further investigation is required to determine its specific uses and the reasons behind them.
Used in Pharmaceutical Industry:
Ethanone, 1-(2-amino-4-pyrimidinyl)-2-bromo(9CI) could potentially be used as a building block or intermediate in the synthesis of pharmaceutical compounds, given its unique chemical structure. Its application in this industry would be for the development of new drugs or the improvement of existing ones, taking advantage of its pyrimidine ring and bromine atom.
Used in Materials Science:
In the field of materials science, Ethanone, 1-(2-amino-4-pyrimidinyl)-2-bromo(9CI) might be employed as a component in the design and synthesis of novel materials with specific properties. Its application in this industry would be for the creation of advanced materials with tailored characteristics, such as improved stability, reactivity, or selectivity.
Used in Chemical Research:
Ethanone, 1-(2-amino-4-pyrimidinyl)-2-bromo(9CI) could also be utilized in chemical research as a subject of study to explore its reactivity, stability, and potential interactions with other compounds. Its application in this context would be for advancing the understanding of pyrimidinones and their role in chemical reactions and processes.

Check Digit Verification of cas no

The CAS Registry Mumber 106157-91-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,1,5 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 106157-91:
(8*1)+(7*0)+(6*6)+(5*1)+(4*5)+(3*7)+(2*9)+(1*1)=109
109 % 10 = 9
So 106157-91-9 is a valid CAS Registry Number.

106157-91-9SDS

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 1-(2-aminopyrimidin-4-yl)-2-bromoethanone

1.2 Other means of identification

Product number -
Other names 1-(2-amino-4-pyrimidinyl)-2-bromo-ethanone hydrobromide

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:106157-91-9 SDS

106157-91-9Relevant academic research and scientific papers

Heteroarylpyrrolopyridinones active as kinase inhibitors

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Page/Page column 17, (2008/06/13)

Compounds represented by formula (I) wherein A, R1, R2, R3, R4, R5 and R6 are as defined in the specification or a pharmaceutically acceptable salt or solvate thereof, compositions thereof,

N-substituted pyrrolopyridinones active as kinase inhibitors

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Page/Page column 19, (2010/11/27)

Compounds represented by formula (I) wherein A, R1, R2, R3, R4, R5, and R6 are as defined in the specification, pharmaceutical compositions thereof, and methods of use thereof.

PYRROLOPYRROLONES ACTIVE AS KINASE INHIBITORS

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Page/Page column 32-33, (2010/11/28)

Compounds represented by formula (I) wherein A, R1, R2, R3, and R4 are as defined in the specification, compositions thereof, and methods of use thereof.

PYRIMIDYLPYRROLE DERIVATIVES ACTIVE AS KINASE INHIBITORS

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Page/Page column 24; 25, (2010/02/10)

Pyrimidylpyrrole derivatives of formula (1) and pharmaceutically acceptable salts thereof, as defined in the specification, process for their preparation and pharmaceutical compositions comprising them are disclosed; the compounds of the invention may be

2-Amino- and 2-Guanidino-4-thiazolylpyrimidines

Lipinski, Christopher A.,Craig, Rebecca H.,Wright, Roger B.

, p. 1723 - 1726 (2007/10/02)

The synthesis of the four possible 2-amino- and 2-guanidino-4-(2-amino- and 2-guanidinothiazolyl)pyrimidines is described and pKa values are calculated.Guanidinopyrimidines are more basic than guanidinothiazoles.However, the reverse is true of the corresponding amino heterocycles; the amino thiazole is more basic than the amino pyrimidine.

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