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[5-bromo-2-(2-methylpyrrolidin-1-yl)phenyl]methanol is a chemical compound characterized by its molecular formula C13H16BrNO. It is a white solid that is prominently utilized in the realms of organic synthesis and medicinal chemistry. [5-bromo-2-(2-methylpyrrolidin-1-yl)phenyl]methanol is distinguished by the presence of a bromine atom and a phenyl ring, to which a methylpyrrolidin-1-yl group is attached. The inclusion of a hydroxyl (OH) functional group indicates its potential applicability in the pharmaceutical industry and as an intermediate in the synthesis of other organic compounds. The specific uses and properties of [5-bromo-2-(2-methylpyrrolidin-1-yl)phenyl]methanol are contingent upon the particular application it is employed in. It holds significant interest for researchers and chemists due to its prospective role in a variety of chemical and pharmaceutical applications.

1243559-12-7

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1243559-12-7 Usage

Uses

Used in Pharmaceutical Industry:
[5-bromo-2-(2-methylpyrrolidin-1-yl)phenyl]methanol is used as an intermediate in the synthesis of various pharmaceutical compounds due to its unique molecular structure and functional groups. The presence of the bromine atom and the phenyl ring, along with the hydroxyl group, allows for further chemical reactions and modifications, making it a valuable building block in the development of new drugs.
Used in Organic Synthesis:
In the field of organic synthesis, [5-bromo-2-(2-methylpyrrolidin-1-yl)phenyl]methanol serves as a key component in the creation of a wide array of organic compounds. Its structural features facilitate its involvement in numerous chemical reactions, enabling the synthesis of a diverse range of molecules with potential applications in various industries.
Used in Research and Development:
[5-bromo-2-(2-methylpyrrolidin-1-yl)phenyl]methanol is also employed as a research compound, allowing scientists and chemists to explore its properties and potential applications further. Its unique structure and functional groups make it an intriguing subject for study, with the possibility of uncovering novel uses and insights into its chemical behavior.

Check Digit Verification of cas no

The CAS Registry Mumber 1243559-12-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,3,5,5 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1243559-12:
(9*1)+(8*2)+(7*4)+(6*3)+(5*5)+(4*5)+(3*9)+(2*1)+(1*2)=147
147 % 10 = 7
So 1243559-12-7 is a valid CAS Registry Number.

1243559-12-7Relevant academic research and scientific papers

OXAZOLE PYRIDINE DERIVATIVES USEFUL AS S1P1 RECEPTOR AGONISTS

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Page/Page column 60, (2010/09/18)

The present invention provides oxadiazole pyridine derivatives of Formula (I), their use as medicaments and their use for treating multiple sclerosis and other diseases

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