139026-44-1 Usage
Chemical structure
1-Adamantyl(phenyl)methanamine is a chemical compound consisting of an adamantyl group and a phenyl group attached to a central methanamine molecule.
Classification
It is a tertiary amine, which means it has three organic groups attached to the central nitrogen atom.
Molecular structure
The compound has a unique molecular structure due to the presence of the adamantyl and phenyl groups.
Steric hindrance
The adamantyl group contributes steric hindrance, which can affect the reactivity and interactions of the compound.
Potential applications
1-Adamantyl(phenyl)methanamine may have potential applications in the synthesis of complex organic molecules and materials.
Pharmaceutical development
It may also be useful in the development of pharmaceuticals and other specialized chemical products.
Further research
Additional uses and properties of 1-adamantyl(phenyl)methanamine in various chemical and industrial applications may be revealed through further research and investigation.
Check Digit Verification of cas no
The CAS Registry Mumber 139026-44-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,0,2 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 139026-44:
(8*1)+(7*3)+(6*9)+(5*0)+(4*2)+(3*6)+(2*4)+(1*4)=121
121 % 10 = 1
So 139026-44-1 is a valid CAS Registry Number.
139026-44-1Relevant articles and documents
Synthesis of a new family of adamantylpyridin-2-amines by palladium-catalyzed amination
Averin, Alexei D.,Ranyuk, Elena R.,Golub, Svetlana L.,Buryak, Alexei K.,Savelyev, Evgenii N.,Orlinson, Boris S.,Novakov, Ivan A.,Beletskaya, Irina P.
, p. 2215 - 2221 (2008/03/28)
Palladium-catalyzed arylation of various adamantane-containing amines with 2-bromopyridine has been studied, and the influence of the phosphane ligand, concentration, and molar ratio of the reagents on the composition of the reaction mixture and on the yield of the target adamantylpyridin-2-amines has been analyzed. The dependence of the formation of N,N-diarylated products on the nature of the starting adamantylamines is shown. Georg Thieme Verlag Stuttgart.
