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1-(4-bromo-3-methylphenyl)cyclobutanol is a chemical compound characterized by its molecular formula C11H13BrO. It is a cyclobutanol derivative, which means it contains a four-membered carbon ring with an attached hydroxyl group and a substituted phenyl group. 1-(4-bromo-3-methylphenyl)cyclobutanol features a bromine atom at the 4-position and a methyl group at the 3-position on the phenyl ring. Its unique molecular structure and potential reactivity make it a compound of interest for various applications, particularly in organic synthesis and pharmaceutical research. 1-(4-bromo-3-methylphenyl)cyclobutanol's properties may also contribute to the development of new materials or serve as a building block for the synthesis of more complex molecules.

1448610-48-7

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1448610-48-7 Usage

Uses

Used in Organic Synthesis:
1-(4-bromo-3-methylphenyl)cyclobutanol is used as an intermediate in organic synthesis for its unique molecular structure and potential reactivity. Its presence of a bromine atom and a methyl group on the phenyl ring allows for further functionalization and the creation of a diverse range of chemical products.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1-(4-bromo-3-methylphenyl)cyclobutanol is used as a starting material or a building block for the development of new drugs. Its specific molecular features may contribute to the design of novel therapeutic agents, particularly those targeting specific biological pathways or receptors.
Used in Material Science:
1-(4-bromo-3-methylphenyl)cyclobutanol's properties may also make it useful in the development of new materials, such as those with unique optical, electronic, or mechanical characteristics. Its potential applications in material science could lead to the creation of innovative products with enhanced performance.
Used in Chemical Research:
1-(4-bromo-3-methylphenyl)cyclobutanol serves as a valuable compound for chemical research, allowing scientists to study its reactivity, stability, and interactions with other molecules. This research can provide insights into the fundamental principles of chemistry and contribute to the advancement of the field.

Check Digit Verification of cas no

The CAS Registry Mumber 1448610-48-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,8,6,1 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1448610-48:
(9*1)+(8*4)+(7*4)+(6*8)+(5*6)+(4*1)+(3*0)+(2*4)+(1*8)=167
167 % 10 = 7
So 1448610-48-7 is a valid CAS Registry Number.

1448610-48-7Relevant academic research and scientific papers

INDOLE AND INDAZOLE COMPOUNDS THAT ACTIVATE AMPK

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Paragraph 0906, (2013/10/22)

The present invention relates to indole and indazole compounds of Formula (I) that activate 5′ adenosine monophosphate-activated protein kinase (AMPK). The invention also encompasses pharmaceutical compositions containing these compounds and methods for treating or preventing diseases, conditions, or disorders ameliorated by activation of AMPK.

HETEROCYCLIC COMPOUNDS AS INHIBITORS OF LEUKOTRIENE PRODUCTION

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Paragraph 0176; 0177; 0178, (2013/08/14)

The present invention relates to compound of formula (I): or pharmaceutically acceptable salts thereof, wherein R1-R7, A and HET are as defined herein. The invention also relates to pharmaceutical compositions comprising these compounds, methods of using these compounds in the treatment of various diseases and disorders, processes for preparing these compounds and intermediates useful in these processes

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