13928-68-2 Usage
General Description
5,7-DIMETHYLADAMANTANE-1,3-DICARBOXYLIC ACID is a chemical compound that contains two carboxylic acid functional groups and a 5,7-dimethyladamantane backbone. It is a derivative of adamantane, a hydrocarbon that has a unique diamondoid structure. 5,7-DIMETHYLADAMANTANE-1,3-DICARBOXYLIC ACID has potential applications in organic synthesis, medicinal chemistry, and material science. Its structure and properties make it a valuable building block for creating new molecules with specific functionality and biological activity. Additionally, its rigid and bulky structure can also influence the physical and chemical properties of materials it is incorporated into, making it useful in the development of advanced materials.
Check Digit Verification of cas no
The CAS Registry Mumber 13928-68-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,2 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13928-68:
(7*1)+(6*3)+(5*9)+(4*2)+(3*8)+(2*6)+(1*8)=122
122 % 10 = 2
So 13928-68-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H20O4/c1-11-3-12(2)6-13(4-11,9(15)16)8-14(5-11,7-12)10(17)18/h3-8H2,1-2H3,(H,15,16)(H,17,18)
13928-68-2Relevant articles and documents
Adamantane-containing esters as potential components of thermostable lubricating oils
Bagrii,Maravin
, (2013)
Some esters of dimethyladamantanedicarboxylic acids with aliphatic alcohols and the ester of dimethyladamantanedicarbinol with an aliphatic acid have been synthesized, and their properties have been studied; their viscosity-temperature properties and ther
The first one-pot synthesis of 1,3-dicarbonyl adamantanes from 1-bromoadamantanes
Akhrem, Irena S.,Avetisyan, Dzhul'Etta V.,Afanas'Eva, Lyudmila V.,Goryunov, Evgenii I.,Churilova, Irina M.,Petrovskii, Pavel V.,Kagramanov, Nikolai D.
experimental part, p. 259 - 261 (2012/07/14)
Treatment of 1-bromoadamantane and 1-bromo-3,5-dimethyladamantane with CBr4·2AlBr3 under carbon monoxide atmosphere followed by quenching with nucleophiles affords 1,3-dicarbonyl adamantanes.
