26460-76-4 Usage
Chemical Family
1-METHYLDIAMANTANE is a chemical compound that belongs to the family of diamantane derivatives.
Structure
It is a saturated hydrocarbon with a unique diamondoid structure.
Appearance
1-METHYLDIAMANTANE is a white crystalline solid.
Uses
It is primarily used as a non-volatile additive in lubricants and fuels to improve their stability and performance.
Stability
1-METHYLDIAMANTANE has excellent thermal and oxidative stability, making it an ideal choice for high-temperature applications.
Growth Inhibitor
It is used as a growth inhibitor for organic thin film deposition processes.
Building Block
1-METHYLDIAMANTANE is used as a building block for the synthesis of advanced materials and pharmaceutical compounds.
Nanotechnology
It has potential applications in the field of nanotechnology.
Diamondoid Materials
1-METHYLDIAMANTANE is a robust building block for the construction of diamondoid materials.
Check Digit Verification of cas no
The CAS Registry Mumber 26460-76-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,4,6 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 26460-76:
(7*2)+(6*6)+(5*4)+(4*6)+(3*0)+(2*7)+(1*6)=114
114 % 10 = 4
So 26460-76-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H22/c1-15-7-9-3-11-10-2-8(5-13(11)15)6-14(15)12(10)4-9/h8-14H,2-7H2,1H3
26460-76-4Relevant articles and documents
Hydrogenolysis of Alkyl-Substituted Adamantanes, Diamantanes, and Triamantanes in the Gas Phase on a Nickel-Alumina Catalyst
Grubmueller, Peter,Maier, Wilhelm F.,Raque Schleyer, Paul von,McKervey, M. Anthony,Rooney, John J.
, p. 1989 - 2006 (2007/10/02)
Dealkylation of several alkyladamantanes, diamantanes, and triamantanes has been observed in the gas phase with hydrogen at atmospheric pressure on a 30percent nickel-alumina catalyst.Yield-temperature profiles show that the optimum temperature for obtaining the pure parent compound in high yield can be as low as 215 deg C.The ease of removal of an alkyl substituent depends on whether it is secondary or tertiary on the diamondoid nucleus.Rupture of the diamondoid skeleton requires much higher temperatures (over 280 deg C) than dealkylation.The hydrogenolytic degradation of diamantane to adamantane was examined with the aid of molecular mechanics calculations; likely pathways for C-C bond cleavage were deduced which are consistent with the several intermediates detected experimentally.The mechanism of dealkylation is discussed in terms of steric and thermodynamic factors and the nature of possible surface intermediates.*
