3114-30-5 Usage
General Description
3',4'-Dibromoacetophenone is a chemical compound with the molecular formula C8H6Br2O. It is a phenyl ketone derivative with two bromine atoms attached at the 3' and 4' positions of the phenyl ring. 3',4'-DIBROMOACETOPHENONE is commonly used in organic synthesis as a building block for the preparation of various pharmaceuticals and agrochemicals. It is also used as an intermediate in the synthesis of dyes, perfumes, and other organic compounds. Additionally, 3',4'-Dibromoacetophenone has been studied for its potential antimicrobial and antifungal properties, as well as its use as a reagent in chemical analysis and research. Overall, this compound plays a critical role in the production of diverse chemicals and has potential applications in various fields.
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 articles and documents
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.
