306935-16-0 Usage
Uses
Used in Pharmaceutical Industry:
3-(Methoxycarbonyl)-2,2,3-trimethylcyclopentane-1-carboxylic acid is used as a chemical intermediate for the synthesis of various pharmaceutical compounds due to its unique structural features and the presence of the ester functional group, which can be utilized in the development of new drugs.
Used in Organic Synthesis:
In the field of organic synthesis, 3-(Methoxycarbonyl)-2,2,3-trimethylcyclopentane-1-carboxylic acid serves as a key building block for the creation of complex organic molecules. Its cyclopentane ring and ester functionality provide a versatile platform for further chemical reactions and modifications, contributing to the synthesis of specialty chemicals and materials.
Used in Material Science:
3-(Methoxycarbonyl)-2,2,3-trimethylcyclopentane-1-carboxylic acid may also find applications in material science, where its unique molecular structure could be leveraged to develop new materials with specific properties. Further research into its potential use in this field could lead to the discovery of novel materials with applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 306935-16-0 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 306935-16:
(8*3)+(7*0)+(6*6)+(5*9)+(4*3)+(3*5)+(2*1)+(1*6)=140
140 % 10 = 0
So 306935-16-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H18O4/c1-10(2)7(8(12)13)5-6-11(10,3)9(14)15-4/h7H,5-6H2,1-4H3,(H,12,13)
306935-16-0Relevant 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.
