845276-75-7 Usage
Description
Methanone, (2-aminophenyl)(2-bromophenyl)-, also known as 2-Amino-2′-bromobenzophenone, is a chemical compound with the molecular formula C13H9BrNO. It is a ketone compound that consists of a benzophenone core with an amino group attached to one phenyl ring and a bromine atom attached to the other phenyl ring.
Uses
Used in Organic Synthesis:
Methanone, (2-aminophenyl)(2-bromophenyl)is used as a building block in organic synthesis for creating various drugs and pharmaceutical products. Its unique structure allows for the formation of diverse chemical compounds through reactions with other molecules.
Used in Pharmaceutical Research:
In pharmaceutical research, Methanone, (2-aminophenyl)(2-bromophenyl)is utilized as a key intermediate in the development of new drugs and pharmaceuticals. Its presence in the molecular structure can contribute to the desired properties and therapeutic effects of the final product.
Used in Dye and Pigment Production:
Methanone, (2-aminophenyl)(2-bromophenyl)is also used in the production of dyes and pigments. Its chemical properties enable the creation of a wide range of colors and shades, making it a valuable component in the dye and pigment industry.
Used in Industrial Chemicals:
Methanone, (2-aminophenyl)(2-bromophenyl)is utilized in the production of various industrial chemicals. Its versatility and reactivity make it suitable for use in different chemical processes and applications.
Used in Materials Science:
Methanone, (2-aminophenyl)(2-bromophenyl)has potential applications in materials science. Its unique structure and properties can be harnessed to develop new materials with specific characteristics and functions.
Used as a Reagent in Chemical Reactions:
In addition to its other uses, Methanone, (2-aminophenyl)(2-bromophenyl)is employed as a reagent in various chemical reactions. Its ability to participate in different types of reactions makes it a valuable tool in the field of chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 845276-75-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,5,2,7 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 845276-75:
(8*8)+(7*4)+(6*5)+(5*2)+(4*7)+(3*6)+(2*7)+(1*5)=197
197 % 10 = 7
So 845276-75-7 is a valid CAS Registry Number.
845276-75-7Relevant articles and documents
Preparation method of 1-bromofluorenone
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, (2021/03/30)
The invention discloses a preparation method of 1-bromo fluorenone, and belongs to the field of organic chemical synthesis. The method is realized by the following steps of: reacting 2-bromophenyl acetonitrile serving as an initial raw material with nitrobenzene to synthesize 3-(2-bromophenyl)-5-benzoisoxazole; reducing 3-(2-bromophenyl)-5-benzoisoxazole by iron powder to obtain 2-aminobenzene-2'-bromobenzophenone, and finally performing intramolecular cyclization to synthesize 1-bromofluorenone with the content of 99.5% (HPLC) or above and the total yield of 76% or above. The synthesis methodis low in production cost and suitable for industrial production, and 1-bromofluorenone can be used in the fields of organic photoelectric materials, biomedicines and dyes.
Pd-NHC catalysed Carbonylative Suzuki coupling reaction and its application towards the synthesis of biologically active 3-aroylquinolin-4 (1H)-one and acridone scaffolds
Ghosh, Prasanjit,Ganguly, Bhaskar,Das, Sajal
, (2018/03/01)
We have unfolded a convenient and mild protocol for the synthesis of diaryl ketones via Pd- NHC catalysed carbonylative Suzuki coupling reaction. Notably, this method offers advantages like no use of toxic CO gas, shorter reaction time, high yield, and broad substrate scope. Several sensitive functional groups (like-COMe, -COOMe, -F, -Cl, -Br, -NH2, -CN) are well tolerated in this reaction. In addition, we have also demonstrated a new efficient route for the synthesis of biologically active and pharmaceutically important 2-substituted 3-Aroylquinolin-4(1H)-ones and acridone scaffolds.
