3114-30-5 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
3',4'-Dibromoacetophenone serves as a crucial building block in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows for the development of new compounds with improved therapeutic and pesticidal properties, contributing to advancements in healthcare and agriculture.
Used in Dye and Perfume Industries:
As an intermediate in the synthesis of dyes and perfumes, 3',4'-Dibromoacetophenone plays a significant role in creating a diverse range of colorants and fragrances. Its chemical properties enable the production of novel dyes with enhanced colorfastness and stability, as well as the creation of unique and complex perfume compositions.
Used in Chemical Analysis and Research:
3',4'-Dibromoacetophenone has been studied for its potential as a reagent in chemical analysis and research. Its unique chemical properties make it a valuable tool for investigating various chemical reactions and processes, contributing to a deeper understanding of chemical phenomena and the development of new analytical techniques.
Used in Antimicrobial and Anti-Fungal Applications:
3',4'-Dibromoacetophenone has been explored for its potential antimicrobial and antifungal properties. Its ability to inhibit the growth of various microorganisms makes it a promising candidate for use in the development of new antimicrobial agents, which could help address the growing issue of antibiotic resistance and improve public health.
Check Digit Verification of cas no
The CAS Registry Mumber 3114-30-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,1 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3114-30:
(6*3)+(5*1)+(4*1)+(3*4)+(2*3)+(1*0)=45
45 % 10 = 5
So 3114-30-5 is a valid CAS Registry Number.
3114-30-5Relevant academic research and scientific papers
Remote electronic effects in the rhodium-catalyzed nucleophilic ring opening of oxabenzonorbornadienes.
Lautens, Mark,Schmid, Gavin A,Chau, Anh
, p. 8043 - 8053 (2007/10/03)
We report the application of our rhodium-catalyzed nucleophilic ring-opening methodology to unsymmetrically arene-substituted oxabenzonorbornadienes. The regioselectivity of the ring opening was investigated using a variety of nucleophiles that led to a broad selection of dihydronaphthalene products. It was found that good to excellent regioselectivities are obtained using strongly pi-donating substituents, whereas sigma-donating and electron-withdrawing functionalities have a minimal effect. Post ring-opening manipulations of functional groups in the dihydronaphthalene products were shown to give efficient access to mono- and diamine tetrahydronaphthalene building blocks.
Production of halo-substituted derivatives of acetophenone
-
, (2008/06/13)
A process for producing halosubstituted derivatives of acetophenone from the respective halocumenes, the term "halo" as used herein, signifying chlorine or bromine, the molecule containing 1 to 3 nuclear halo substituents in the meta- and/or paraposition relative to the isopropyl group. The process comprises oxidizing the halocumene by means of air or oxygen. The oxidation is effected in the presence of a metal phthalocyanine complex as catalyst, and in a most preferred embodiment, in the co-presence of a dichlorobenzene solvent. The preferred halocumenes are p-chlorocumene and p-bromocumene.
