19816-96-7 Usage
Uses
Used in Organic Synthesis:
2,4,6-Cycloheptatrien-1-one, O-[(4-methylphenyl)sulfonyl]oxime is used as a reagent in organic synthesis for the preparation of other organic compounds. Its unique structure and properties make it a valuable component in the creation of a variety of chemical entities.
Used in Perfume and Fragrance Industry:
In the perfume and fragrance industry, 2,4,6-Cycloheptatrien-1-one, O-[(4-methylphenyl)sulfonyl]oxime is used as a scent ingredient for its strong odour. Its distinctive aroma contributes to the formulation of various fragrances and scents in consumer products.
Used in Pharmaceutical Applications:
2,4,6-Cycloheptatrien-1-one, O-[(4-methylphenyl)sulfonyl]oxime is studied for its potential biological activities and is used as a candidate in pharmaceutical research. Its exploration in this field aims to identify possible therapeutic uses and applications in medicine.
Used in Chemical Reactions:
As a reagent, 2,4,6-Cycloheptatrien-1-one, O-[(4-methylphenyl)sulfonyl]oxime is utilized in various chemical reactions to facilitate specific transformations or syntheses. Its role in these processes is crucial for achieving desired outcomes in chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 19816-96-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,1 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 19816-96:
(7*1)+(6*9)+(5*8)+(4*1)+(3*6)+(2*9)+(1*6)=147
147 % 10 = 7
So 19816-96-7 is a valid CAS Registry Number.
19816-96-7Relevant academic research and scientific papers
A novel synthesis of trienes by nucleophilic ring cleavage of tropone oxime tosylate
Machiguchi, Takahisa,Wada, Yoshiyuki,Hasegawa, Toshio,Yamabe, Shinichi,Minato, Tsutomu,Nozoe, Tetsuo
, p. 1258 - 1264 (2007/10/02)
In contrast to chemical reactions of troponoid ([7]annulenone) compounds reported so far, the tosylate of tropone oxime reveals a novel ring opening reaction under mild conditions at the temperature between -20 and 0 °C. This nucleophilic reaction affords
