831-67-4 Usage
Uses
Used in Pharmaceutical Industry:
Cycloundecanecarboxylic acid is utilized as a precursor in the synthesis of various pharmaceuticals. Its unique ring structure and carboxylic acid group make it a valuable component in the development of new drugs, contributing to the creation of molecules with specific therapeutic properties.
Used in Polymer Industry:
CYCLOUNDECANECARBOXYLIC ACID also serves as a precursor in the production of polymers. Its structural characteristics allow it to be incorporated into polymer chains, potentially influencing the polymer's properties such as strength, flexibility, and durability.
Used as a Corrosion Inhibitor:
Cycloundecanecarboxylic acid finds application as a corrosion inhibitor, protecting metals from degradation in various industrial settings. Its chemical properties enable it to form a protective layer on metal surfaces, thereby preventing corrosion and extending the life of metal components.
Used in Fragrance and Flavor Industry:
Additionally, Cycloundecanecarboxylic acid is employed as an intermediate in the production of fragrances and flavors. Its ability to be modified and incorporated into complex organic molecules makes it a useful component in creating a diverse range of scents and tastes for various consumer products.
Overall, Cycloundecanecarboxylic acid's applications span across multiple industries, highlighting its significance as a versatile intermediate in organic synthesis and its potential for further development in material science and chemical engineering.
Check Digit Verification of cas no
The CAS Registry Mumber 831-67-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 831-67:
(5*8)+(4*3)+(3*1)+(2*6)+(1*7)=74
74 % 10 = 4
So 831-67-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H22O2/c13-12(14)11-9-7-5-3-1-2-4-6-8-10-11/h11H,1-10H2,(H,13,14)
831-67-4Relevant academic research and scientific papers
Oxidative ring contraction of cycloalkanones: A facile metrod for synthesis of medium ring cycloalkanecarboxylic acids
Giurg, Miroslaw,Mlochowski, Jacek
, p. 2281 - 2291 (2007/10/03)
Cycloalkanones (1) oxidized with 30% hydrogen peroxide in the presence of poly(bisanthracenyl) diselenide (5b) as catalyst, produce cycloalkanecarboxylic acids (2) having one carbon atom less in the ring that the substrate. Although preparative yield of acids 2 does not exceed 60% the reaction can be applied as a simple way for synthesis of cycloalkanecarboxylic acids with five to seven-membered ring.
NEW METHOD FOR THE PRODUCTION OF 1,4-DIOXACYCLOHEXADECANE-5,16-DIONE FROM CYCLODECANONE
Zakharkin, L. I.,Guseva, V. V.
, p. 115 - 118 (2007/10/02)
A new method is proposed for the synthesis of 1,4-dioxacyclohexadecane-5,16-dione by the oxidation of 13,16-dioxabicyclohexadec-1(12)-ene, obtained from 2-hydroxycyclododecanone and ethylene glycol.The action of an aqueous or alcohol solution of potassium hydroxide on 2-acetoxy- or 2-hydroxycyclododecanone leads to oxidative cleavage of the C-C bond with the formation of 1,10-decanedicarboxylic acid.
