306935-15-9 Usage
Uses
Used in Pharmaceutical Industry:
3-(METHOXYCARBONYL)-1,2,2-TRIMETHYLCYCLOPENTANE-1-CARBOXYLIC ACID is used as a reactant for the preparation of isothiazolylidene containing compounds. These compounds are known as therapeutic cannabinoid receptor ligands, which have potential applications in the treatment of various medical conditions, such as pain management, anxiety, and neurological disorders.
Used in Chemical Synthesis:
In the field of chemical synthesis, 3-(METHOXYCARBONYL)-1,2,2-TRIMETHYLCYCLOPENTANE-1-CARBOXYLIC ACID can be utilized as a building block or intermediate for the synthesis of more complex organic molecules. Its unique structure and functional groups make it a valuable component in the development of new compounds with specific properties and applications.
Used in Research and Development:
Due to its unique chemical structure, 3-(METHOXYCARBONYL)-1,2,2-TRIMETHYLCYCLOPENTANE-1-CARBOXYLIC ACID can be employed in research and development for the exploration of new chemical reactions, mechanisms, and pathways. It can serve as a model compound for understanding the reactivity and behavior of similar organic molecules, contributing to the advancement of chemical knowledge and innovation.
Check Digit Verification of cas no
The CAS Registry Mumber 306935-15-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,6,9,3 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 306935-15:
(8*3)+(7*0)+(6*6)+(5*9)+(4*3)+(3*5)+(2*1)+(1*5)=139
139 % 10 = 9
So 306935-15-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H18O4/c1-10(2)7(8(12)15-4)5-6-11(10,3)9(13)14/h7H,5-6H2,1-4H3,(H,13,14)
306935-15-9Relevant academic research and scientific papers
Photooxygenation of the C=N bond: A mild new method for oxidative C-C cleavage
?cal, Nüket,Yano, Lovelle M.,Erden, Ihsan
, p. 6947 - 6949 (2007/10/03)
Upon photooxygenation in the presence of base, α-oximinocarbonyl compounds undergo clean oxidative C-C cleavage giving rise to mixtures of esters and acids. The mechanism of these reactions involves some unusual peroxidic intermediates, including a 2,3,5-trioxapentanes.
