116145-28-9 Usage
Description
(2-BROMO-4,5-DIMETHOXYPHENYL)ACETONE is a chemical compound with the molecular formula C11H13BrO3. It is a derivative of acetone with two methoxy groups and a bromine atom attached to a phenyl group. (2-BROMO-4,5-DIMETHOXYPHENYL)ACETONE is known for its versatility in various chemical reactions due to the presence of bromine and methoxy groups.
Uses
Used in Pharmaceutical Industry:
(2-BROMO-4,5-DIMETHOXYPHENYL)ACETONE is used as an intermediate in the synthesis of pharmaceuticals for its ability to be incorporated into the structure of various medicinal compounds. Its unique functional groups allow for the development of new drugs with potential therapeutic benefits.
Used in Organic Compounds Synthesis:
In the field of organic chemistry, (2-BROMO-4,5-DIMETHOXYPHENYL)ACETONE serves as a building block for the production of various aromatic compounds. Its reactivity and structural features make it a valuable component in creating complex organic molecules for research and industrial applications.
Used in Chemical Research:
(2-BROMO-4,5-DIMETHOXYPHENYL)ACETONE is utilized in chemical research to explore its properties and potential applications. Its unique structure allows scientists to study its reactivity, stability, and interactions with other compounds, leading to a better understanding of its role in chemical reactions and potential uses.
It is important to handle and use (2-BROMO-4,5-DIMETHOXYPHENYL)ACETONE with proper safety precautions, as it may pose health and environmental hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 116145-28-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,1,4 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 116145-28:
(8*1)+(7*1)+(6*6)+(5*1)+(4*4)+(3*5)+(2*2)+(1*8)=99
99 % 10 = 9
So 116145-28-9 is a valid CAS Registry Number.
116145-28-9Relevant articles and documents
SYNTHESIS AND REACTIONS OF 2-ARYL-8-OXABICYCLOOCT-6-EN-3-ONES
Mann, John,Wilde, Philip D.,Finch, Mark W.
, p. 5431 - 5442 (2007/10/02)
A number of 1-aryl-1-bromopropanones have been prepared and converted into the corresponding oxyallyl carbocations.These were reacted with furan to produce the expected 2-aryl-8-oxabicyclooct-6-en-3-ones, as well as a number of interesting side-products.These included 3-aryl-propanoic acid esters produced via Favorskii rearrangements.Attempts to cleave the ether linkage in the cycloadducts using bromotrimethylsilane produced instead 1-aryl-3-furylpropanones in excellent yield.
