1305324-47-3 Usage
Uses
Used in Organic Synthesis:
1-(2-Bromo-4-chlorophenyl)propan-2-one is used as a building block for the synthesis of various complex organic molecules. Its unique structure and properties make it a valuable intermediate in the production of different chemical compounds, contributing to the advancement of organic chemistry.
Used in Pharmaceutical Industry:
Due to its structure and properties, 1-(2-Bromo-4-chlorophenyl)propan-2-one has potential applications in the pharmaceutical industry. It can be utilized as a key intermediate in the synthesis of pharmaceutical compounds, potentially leading to the development of new drugs with improved therapeutic effects.
Used in Agrochemical Industry:
1-(2-Bromo-4-chlorophenyl)propan-2-one may also find applications in the agrochemical industry. Its unique structure could be employed in the development of new agrochemicals, such as pesticides or herbicides, that offer enhanced efficacy and selectivity in controlling pests and weeds.
Check Digit Verification of cas no
The CAS Registry Mumber 1305324-47-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,5,3,2 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1305324-47:
(9*1)+(8*3)+(7*0)+(6*5)+(5*3)+(4*2)+(3*4)+(2*4)+(1*7)=113
113 % 10 = 3
So 1305324-47-3 is a valid CAS Registry Number.
1305324-47-3Relevant academic research and scientific papers
SUBSTITUTED OXOPYRIDINE DERIVATIVES
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Page/Page column 64-65, (2020/07/14)
The invention relates to substituted oxopyridine derivatives and to processes for their preparation, and also to their use for preparing medicaments for the treatment and/or prophylaxis of diseases, in particular vascular disorders, preferably thrombotic
Intramolecular Acetyl Transfer to Olefins by Catalytic C?C Bond Activation of Unstrained Ketones
Rong, Zi-Qiang,Lim, Hee Nam,Dong, Guangbin
, p. 475 - 479 (2018/02/21)
A rhodium-catalyzed intramolecular acetyl-group transfer has been achieved through a “cut and sew” process. The challenge arises from the existence of different competitive pathways. Preliminary success has been achieved with unstrained enones that contain a biaryl linker. The use of an electron-rich N-heterocycilc carbene (NHC) ligand is effective to inhibit undesired β-hydrogen elimination. Various 9,10-dihydrophenanthrene derivatives can be prepared with excellent functional-group compatibility. The 13C-labelling study suggests that the reaction begins with cleavage of the unstrained C?C bond, followed by migratory insertion and reductive elimination.
