699-41-2 Usage
Uses
Used in Organic Synthesis:
Ethanone, 1-(1,2-dihydroxycyclohexyl)-, cisis used as a key intermediate in organic synthesis for the preparation of various chemical compounds. Its unique structure and functional groups make it a versatile building block for the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
Ethanone, 1-(1,2-dihydroxycyclohexyl)-, cisis used as a starting material for the synthesis of pharmaceuticals. Its specific configuration and reactivity allow for the development of novel drug candidates with potential therapeutic applications.
Used in Fine Chemicals Production:
In the fine chemicals industry, Ethanone, 1-(1,2-dihydroxycyclohexyl)-, cisis utilized as a precursor for the production of specialty chemicals. Its unique properties enable the creation of high-value products with specific applications in various fields.
Used in Chemical Research:
Ethanone, 1-(1,2-dihydroxycyclohexyl)-, cisserves as a valuable compound for chemical research, particularly in the study of reaction mechanisms, stereochemistry, and the development of new synthetic methodologies. Its unique structure and properties provide insights into the behavior of similar compounds and contribute to the advancement of chemical science.
Check Digit Verification of cas no
The CAS Registry Mumber 699-41-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 699-41:
(5*6)+(4*9)+(3*9)+(2*4)+(1*1)=102
102 % 10 = 2
So 699-41-2 is a valid CAS Registry Number.
699-41-2Relevant academic research and scientific papers
Induced halogenation of alkyl cyclohexenyl ketones involving metal halides, hydrohalogenic acids, and hydrogen peroxide
Sadygov,Alimardanov
experimental part, p. 166 - 172 (2009/09/25)
The induced halogenation and hydroxyhalogenation of alkyl cyclohexenyl ketones in a system [MHlg + HHlg or HHlg]-H2O2 or in NaOCl was performed and optimum reaction conditions were established. Under mild conditions the electrophilic addition of the halogen or the acid occurred at the multiple bond of the ring with the formation of the corresponding dihalo or hydroxyhalo derivatives of cycloaliphatic ketones. From the compounds obtained epoxy- and dioxyketones of aliphatic series were prepared. Chloro(bromo)hydrins of ketones from the alkylcyclohexane series and oxiranes based thereon are reactive compounds and can be employed as synthons in the organic synthesis.
