35223-32-6 Usage
General Description
1-(5-bromo-1,2-dihydroacenaphthylen-3-yl)ethanone is a chemical compound with the molecular formula C14H13BrO. It is a yellowish solid with a molecular weight of 285.16 g/mol. 1-(5-bromo-1,2-dihydroacenaphthylen-3-yl)ethanone is primarily used in research and laboratory settings as a reagent in organic synthesis. It is known for its ability to undergo various chemical reactions, including acylation and bromination. Additionally, it has been studied for its potential pharmaceutical applications, particularly in the development of new drugs and medications. Overall, 1-(5-bromo-1,2-dihydroacenaphthylen-3-yl)ethanone is a versatile compound with a range of potential uses in the fields of chemistry and pharmaceutical science.
Check Digit Verification of cas no
The CAS Registry Mumber 35223-32-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,2,2 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 35223-32:
(7*3)+(6*5)+(5*2)+(4*2)+(3*3)+(2*3)+(1*2)=86
86 % 10 = 6
So 35223-32-6 is a valid CAS Registry Number.
35223-32-6Relevant articles and documents
Reaction of substituted 5-bromoacenaphthenes with the catalytic reduction system NiCl2-2,2'-bipyridyl (or 1,10-phenanthroline)-Zn
Adonin,Ryabinin,Starichenko
, p. 913 - 915 (2007/10/03)
Transformations of substituted 5-bromoacenaphthenes under the action of a catalytic reduction system NiCl2-2,2'-bipyridyl (or 1,10-phenanthrolyne)-Zn in DMF and DMA was studied. Two types of transformation are shown to be characteristic for the studied compounds: reductive coupling with formation of the corresponding 5,5'-biacenaphthenyl and halogen elimination with hydrogen replacing the halogen. Yields of the coupling products and that of dehalogenation are found to depend substantially on the nature of the substituents in the nanhfhalene ring.
