31483-97-3 Usage
Uses
Used in Organic Synthesis:
(2E)-bicyclo[3.2.1]octan-2-one oxime is used as a versatile intermediate for the synthesis of various organic compounds. Its unique structure and functional groups facilitate a range of chemical reactions, making it a key component in the creation of complex molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, (2E)-bicyclo[3.2.1]octan-2-one oxime is used as a building block for the development of new drugs. Its oxime functional group allows for the attachment of various pharmacophores, contributing to the discovery of novel therapeutic agents.
Used in Agrochemical Development:
(2E)-bicyclo[3.2.1]octan-2-one oxime is also utilized in the agrochemical sector as a precursor for the synthesis of pesticides and other crop protection agents. Its ability to undergo further chemical reactions enables the creation of effective and targeted agrochemicals.
Used in Fragrance Industry:
In the fragrance industry, (2E)-bicyclo[3.2.1]octan-2-one oxime is used as a starting material for the production of unique and complex scents. Its chemical properties allow for the creation of a diverse array of fragrance compounds.
Used in Insecticide and Antibacterial Applications:
(2E)-bicyclo[3.2.1]octan-2-one oxime has been studied for its potential biological activities and has shown promise as both an insecticide and an antibacterial agent. Its use in these applications is based on its ability to target and disrupt essential biological processes in pests and bacteria, offering a new avenue for pest and disease control.
Check Digit Verification of cas no
The CAS Registry Mumber 31483-97-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,4,8 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 31483-97:
(7*3)+(6*1)+(5*4)+(4*8)+(3*3)+(2*9)+(1*7)=113
113 % 10 = 3
So 31483-97-3 is a valid CAS Registry Number.
31483-97-3Relevant academic research and scientific papers
Krow, Grant R.,Szczepanski, Steven
, p. 1153 - 1156 (1982)
Earlier reports of totally regioselective bridgehead nitrogen insertion upon rearrangement of the oxime of bicyclooctan-2-one (1), by using benzenesulfonyl chloride/sodium hydroxide as a Beckman catalyst, but completely regioselective methylene migration upon reaction of ketone 1 with hydroxylamine hydrogen sulfate in sulfuric acid have been found to be inaccurate.Lactams 3, formed by bridgehead migration, and 4, arising from methylene migration, are afforded under both sets of reaction conditions as shown by 1H and 13C NMR analyses of crude reaction mixtures.Upon examination of a number of nitrogen insertion reaction conditions, the most regioselective formation of bridgehead nitrogen insertion product 3 (95percent) can be effected by reacting ketone 1 with hydroxylamine-O-sulfonic acid in formic acid.The preference for nitrogen insertion adjacent to methylene was highest for reaction of ketone 1 with hydroxylamine hydrochloride/sulfuric acid which gave a 69percent preference for lactam 4.This exceeds the methylene migratory preference for the Schmidt reaction of ketone 1 with hydrazoic acid, which gives 62percent lactam 4.
