55057-87-9 Usage
Uses
Used in Organic Synthesis:
(1R)-3-bromo-1,7,7-trimethyl-norbornan-2-one is used as a building block in organic synthesis for the preparation of various organic compounds.
Used in Pharmaceutical Production:
(1R)-3-bromo-1,7,7-trimethyl-norbornan-2-one is used as an intermediate in the production of pharmaceuticals due to its unique structure and reactivity.
Used in Agrochemical Production:
(1R)-3-bromo-1,7,7-trimethyl-norbornan-2-one is used as an intermediate in the production of agrochemicals, contributing to the development of effective and targeted products.
Used in Fine Chemicals Production:
(1R)-3-bromo-1,7,7-trimethyl-norbornan-2-one is used as an intermediate in the production of other fine chemicals, showcasing its versatility and importance in various chemical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 55057-87-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,0,5 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 55057-87:
(7*5)+(6*5)+(5*0)+(4*5)+(3*7)+(2*8)+(1*7)=129
129 % 10 = 9
So 55057-87-9 is a valid CAS Registry Number.
55057-87-9Relevant academic research and scientific papers
New chiral cyclopalladated complexes based on the pinane and bornane imines
Kuchin,Gur'eva,Frolova,Alekseev,Zalevskaya
, p. 745 - 750 (2014/01/23)
2α-Hydroxypinan-3-one imino derivatives react with lithium tetrachloropalladate to form palladacycles, while similar bornane derivative undergo cyclopalladation only when treated with palladium acetate.
REACTIVITY OF 3-BROMOCAMPHOR AND 3-BROMOISOCAMPHANONE UNDER THE CONDITIONS OF THE RITTER REACTION
Koval'skaya, S. S.,Kozlov, N. G.,Zyryanov, V. A.
, p. 722 - 726 (2007/10/02)
The bromination of camphor and isocamphanone yield, respectively, 3-endo- and 3-exo-bromo ketones.Under the conditions of the Ritter reaction 3-bromocamphor does not react with nitriles, while 3-isocamphanone is selectively converted into the corresponding N,N'-diacyl-3-bromo-2,2-gem-diamino-5,5,6-trimethylbicycloheptanes.
Correlation of nuclear magnetic resonance spectra and structure of trans-camphane-2,3-diols
Allen, M. S.,Hutchinson, J. H.,Money, T.
, p. 2707 - 2708 (2007/10/02)
Evidence is provided to demonstrate that a recent correction in the published nmr spectra of trans-camphane-2,3-diols is unjustified
