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1-(4-bromophenyl)-2-(isoquinolin-1-ylsulfanyl)ethanone is a chemical compound characterized by a molecular structure that features a 4-bromophenyl group connected to a sulfur-containing isoquinoline ring. As an ethanone, it possesses a ketone functional group, which may contribute to its reactivity and potential applications in medicinal chemistry and drug discovery. The unique structure of 1-(4-bromophenyl)-2-(isoquinolin-1-ylsulfanyl)ethanone, including the presence of bromine and sulfur atoms, suggests that it could interact with biological targets in a specific manner, making it a promising candidate for further research and development in the pharmaceutical industry.

13896-95-2

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13896-95-2 Usage

Uses

Used in Medicinal Chemistry:
1-(4-bromophenyl)-2-(isoquinolin-1-ylsulfanyl)ethanone is used as a chemical compound in medicinal chemistry for its potential to interact with specific biological targets. Its unique structure, including the bromine and sulfur atoms, may contribute to its reactivity and pharmacological properties, making it a valuable tool for the development of new therapeutic agents.
Used in Drug Discovery:
In the field of drug discovery, 1-(4-bromophenyl)-2-(isoquinolin-1-ylsulfanyl)ethanone is used as a starting point for the development of new therapeutic agents. Its molecular structure and functional groups may be optimized to enhance its interactions with biological targets, potentially leading to the discovery of novel drugs with improved efficacy and selectivity.
Used in Chemical Tools Development:
1-(4-bromophenyl)-2-(isoquinolin-1-ylsulfanyl)ethanone is also used as a chemical tool for studying biological systems. Its unique structure and reactivity may allow researchers to probe the function and interactions of various biological targets, providing valuable insights into the underlying mechanisms of disease and the development of targeted therapies.
Used in Pharmaceutical Industry:
Within the pharmaceutical industry, 1-(4-bromophenyl)-2-(isoquinolin-1-ylsulfanyl)ethanone is used as a key intermediate in the synthesis of various drug candidates. Its potential reactivity and pharmacological properties make it a valuable component in the development of new medications, particularly those targeting specific biological pathways or receptors.

Check Digit Verification of cas no

The CAS Registry Mumber 13896-95-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,9 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13896-95:
(7*1)+(6*3)+(5*8)+(4*9)+(3*6)+(2*9)+(1*5)=142
142 % 10 = 2
So 13896-95-2 is a valid CAS Registry Number.

13896-95-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-bromophenacylpyridinium iodide

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

Emergency phone number -
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More Details:13896-95-2 SDS

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