15291-66-4 Usage
Uses
Used in Pharmaceutical and Agrochemical Synthesis:
3,5,7-Trimethyladamantane-1-carboxylic acid is used as a building block for the synthesis of various pharmaceuticals and agrochemicals. Its unique steric hindrance and rigid structure contribute to the development of novel compounds with improved properties and efficacy.
Used in Material and Polymer Development:
3,5,7-TRIMETHYLADAMANTANE-1-CARBOXYLIC ACID is utilized in the development of new materials and polymers due to its rigid and bulky structure, which can impart unique properties to the resulting materials.
Used as an Antioxidant:
3,5,7-Trimethyladamantane-1-carboxylic acid is used as an antioxidant, helping to protect cells and tissues from oxidative damage caused by reactive oxygen species. Its antioxidant properties can be beneficial in various applications, including healthcare and industrial processes.
Used as an Anti-inflammatory Agent:
3,5,7-TRIMETHYLADAMANTANE-1-CARBOXYLIC ACID is used as an anti-inflammatory agent, exhibiting potential to reduce inflammation and alleviate symptoms associated with inflammatory conditions.
Used in Drug Delivery Systems:
3,5,7-Trimethyladamantane-1-carboxylic acid is being studied for its potential application in drug delivery systems. Its unique structure and properties may enable the development of novel drug delivery platforms, improving the efficacy and targeting of therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 15291-66-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,2,9 and 1 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15291-66:
(7*1)+(6*5)+(5*2)+(4*9)+(3*1)+(2*6)+(1*6)=104
104 % 10 = 4
So 15291-66-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H22O2/c1-11-4-12(2)6-13(3,5-11)9-14(7-11,8-12)10(15)16/h4-9H2,1-3H3,(H,15,16)
15291-66-4Relevant academic research and scientific papers
Reaction of Adamantane Alcohols with Bromine
Baklan,Khil'chevskii,Kukhar'
, p. 498 - 505 (2007/10/03)
1-Hydroxyadamantane and 1-hydroxy-3,5,7-trimethyladamantane in the medium of liquid bromine are converted, correspondingly, into 1-bromoadamantane and 1-bromo-3,5,7-trimethyladamantane by substitution of the hydroxy group with molecular bromine. 1-Hydroxyalkyl derivatives of adamantane afford alkyl bromides by means of substitution of the hydroxy groups for bromine with both molecular bromine and, possibly, hydrogen bromide formed upon oxidation of alcohols with bromine. A scheme of substitution of the hydroxy group with molecular bromine is suggested.
Xi:Irritant;
