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(2R)-2-(6-bromo-2-methoxyquinolin-3-yl)-1-(naphthalen-1-yl)-2-phenylethanone is a complex organic compound characterized by its unique molecular structure. It features a naphthalene group, a phenyl group, and a quinolin-3-yl group, all of which contribute to its potential biological activity. As a ketone, it contains a carbonyl group (C=O) and a chiral center (2R), which may influence its reactivity and stereochemistry. Additionally, the presence of a bromine atom and a methoxy group further diversifies its chemical properties and possible applications.

1298044-25-3

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1298044-25-3 Usage

Uses

Used in Pharmaceutical Research:
(2R)-2-(6-bromo-2-methoxyquinolin-3-yl)-1-(naphthalen-1-yl)-2-phenylethanone is used as a research compound for exploring its potential biological activity and therapeutic effects. The presence of a quinolin-3-yl group, which is found in some drugs and bioactive compounds, suggests that (2R)-2-(6-bromo-2-methoxyquinolin-3-yl)-1-(naphthalen-1-yl)-2-phenylethanone may have applications in the development of new pharmaceuticals.
Used in Chemical Synthesis:
In the chemical industry, (2R)-2-(6-bromo-2-methoxyquinolin-3-yl)-1-(naphthalen-1-yl)-2-phenylethanone can be used as an intermediate in the synthesis of more complex molecules. Its unique structure, including the carbonyl group and the chiral center, may be exploited in the creation of novel compounds with specific properties.
Used in Biochemical Studies:
Due to its complex structure and the presence of various functional groups, (2R)-2-(6-bromo-2-methoxyquinolin-3-yl)-1-(naphthalen-1-yl)-2-phenylethanone may also be utilized in biochemical studies to investigate its interactions with biological systems. This could include examining its binding to specific proteins, enzymes, or other biomolecules, which may reveal insights into its potential uses in medicine or other fields.
Used in Material Science:
(2R)-2-(6-bromo-2-methoxyquinolin-3-yl)-1-(naphthalen-1-yl)-2-phenylethanone's structural features may also lend itself to applications in material science, where it could be explored for its potential to influence the properties of new materials. For example, its incorporation into polymers or other composites might result in materials with unique characteristics, such as improved stability, reactivity, or selectivity in certain applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1298044-25-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,8,0,4 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1298044-25:
(9*1)+(8*2)+(7*9)+(6*8)+(5*0)+(4*4)+(3*4)+(2*2)+(1*5)=173
173 % 10 = 3
So 1298044-25-3 is a valid CAS Registry Number.

1298044-25-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-2-(6-bromo-2-methoxyquinolin-3-yl)-1-(naphthalen-1-yl)-2-phenylethanone

1.2 Other means of identification

Product number -
Other names -

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

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More Details:1298044-25-3 SDS

1298044-25-3Relevant academic research and scientific papers

Practical syntheses of (2S)-R207910 and (2R)-R207910

Chandrasekhar, Srivari,Babu, G. S. Kiran,Mohapatra, Debendra K.

, p. 2057 - 2061 (2011/05/09)

Concise and practical syntheses of (2S)-R207910 (3a) and (2R)-R207910 (3b) have been achieved in high overall yield of 12 % in 10 steps for each isomer starting from a known intermediate following Sharpless asymmetric epoxidation, regioselective epoxide opening, modified allylzinc bromide addition as key reactions. Copyright

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