175136-42-2 Usage
Uses
Used in Medicinal Chemistry:
(7-BROMO-2,3-DIHYDRO-1,4-BENZODIOXIN-6-YL)(4-METHYLPHENYL)METHANONE is used as a chemical intermediate for the synthesis of pharmaceutical compounds due to its unique structure and potential reactivity, which may contribute to the development of new drugs with novel mechanisms of action.
Used in Pharmacology Research:
In the field of pharmacology, (7-BROMO-2,3-DIHYDRO-1,4-BENZODIOXIN-6-YL)(4-METHYLPHENYL)METHANONE is utilized as a research tool to study its interactions with biological systems, potentially leading to insights into new therapeutic targets or the discovery of its own pharmacological activity.
Used in Chemical Synthesis:
(7-BROMO-2,3-DIHYDRO-1,4-BENZODIOXIN-6-YL)(4-METHYLPHENYL)METHANONE serves as a key component in the synthesis of complex organic compounds, where its specific functional groups can be manipulated to create a variety of derivatives with different properties and applications.
Used in Material Science:
In material science, (7-BROMO-2,3-DIHDRO-1,4-BENZODIOXIN-6-YL)(4-METHYLPHENYL)METHANONE may be explored for its potential to contribute to the development of new materials with unique electronic, optical, or mechanical properties, given its structural features.
Check Digit Verification of cas no
The CAS Registry Mumber 175136-42-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,1,3 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 175136-42:
(8*1)+(7*7)+(6*5)+(5*1)+(4*3)+(3*6)+(2*4)+(1*2)=132
132 % 10 = 2
So 175136-42-2 is a valid CAS Registry Number.
InChI:InChI=1/C16H13BrO3/c1-10-2-4-11(5-3-10)16(18)12-8-14-15(9-13(12)17)20-7-6-19-14/h2-5,8-9H,6-7H2,1H3
175136-42-2Relevant academic research and scientific papers
Mochalov,Fedotov,Trofimova,Zefirov
, p. 403 - 413 (2018)
2-Cyanobenzophenones were synthesized by reaction of 2-bromobenzophenones with copper(I) cyanide in DMF, and their transformations involving acid hydrolysis of the cyano group were studied. Reactions of o-benzoylbenzonitriles with trifluoroacetic acid in
