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1298044-24-2

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  • (2R)-2-(6-bromo-2-methoxyquinolin-3-yl)-1-(naphthalen-1-yl)-2-phenylethanol

    Cas No: 1298044-24-2

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1298044-24-2 Usage

Description

3-Quinolineethanol, 6-bromo-2-methoxy-α-1-naphthalenyl-β-phenyl-, (βR)-, also known as 6-Bromo-2-methoxy-α-naphthyl-β-phenylethanol, is a chiral chemical compound with the molecular formula C25H21BrO2. It is characterized by its specific stereochemistry, represented by the (βR)designation. 3-Quinolineethanol, 6-bromo-2-methoxy-α-1-naphthalenyl-β-phenyl-, (βR)is utilized in research and development, especially within the pharmaceutical industry, due to its potential therapeutic properties and applications in treating inflammation, cancer, and neurological disorders.

Uses

Used in Pharmaceutical Industry:
3-Quinolineethanol, 6-bromo-2-methoxy-α-1-naphthalenyl-β-phenyl-, (βR)is used as a research compound for its potential therapeutic properties in the development of new drugs. Its chiral nature allows for the exploration of different pharmacological effects based on its stereochemistry, which is crucial for drug development and medicinal chemistry.
Used in Inflammation Research:
In the field of inflammation, 3-Quinolineethanol, 6-bromo-2-methoxy-α-1-naphthalenyl-β-phenyl-, (βR)is employed as a research tool to study its potential anti-inflammatory effects and to understand its role in modulating inflammatory processes.
Used in Cancer Research:
3-Quinolineethanol, 6-bromo-2-methoxy-α-1-naphthalenyl-β-phenyl-, (βR)is used as a compound of interest in cancer research, where it is being investigated for its potential to target and treat various types of cancer by affecting specific cellular pathways and mechanisms.
Used in Neurological Disorders Research:
In the area of neurological disorders, 3-Quinolineethanol, 6-bromo-2-methoxy-α-1-naphthalenyl-β-phenyl-, (βR)is utilized as a research molecule to explore its potential in treating or managing neurological conditions, given its possible interaction with specific neurological pathways and receptors.

Check Digit Verification of cas no

The CAS Registry Mumber 1298044-24-2 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 1298044-24:
(9*1)+(8*2)+(7*9)+(6*8)+(5*0)+(4*4)+(3*4)+(2*2)+(1*4)=172
172 % 10 = 2
So 1298044-24-2 is a valid CAS Registry Number.

1298044-24-2SDS

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-phenylethanol

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:1298044-24-2 SDS

1298044-24-2Relevant articles and documents

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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