3717-44-0 Usage
General Description
N-ethyl-1-adamantanamine, also known as ethylaminoadamantane, is an organic compound with the molecular formula C12H21N. It is a derivative of the alicyclic amine adamantane, and its structure consists of a central adamantane core with an ethylamine group attached at the 1-position. N-ethyl-1-adamantanamine has various pharmacological properties and has been studied for its potential use as an antiviral and antiparkinsonian agent. It is also used as a precursor in the synthesis of other organic compounds. Additionally, it has been investigated for its potential use in the treatment of drug addiction and neuroprotection.
Check Digit Verification of cas no
The CAS Registry Mumber 3717-44-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,1 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3717-44:
(6*3)+(5*7)+(4*1)+(3*7)+(2*4)+(1*4)=90
90 % 10 = 0
So 3717-44-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H21N/c1-2-13-12-6-9-3-10(7-12)5-11(4-9)8-12/h9-11,13H,2-8H2,1H3
3717-44-0Relevant articles and documents
Catalytic N-Alkylation of Amines Using Carboxylic Acids and Molecular Hydrogen
Sorribes, Iván,Cabrero-Antonino, Jose R.,Vicent, Cristian,Junge, Kathrin,Beller, Matthias
supporting information, p. 13580 - 13587 (2015/11/10)
A convenient, practical and green N-alkylation of amines has been accomplished by applying readily available carboxylic acids in the presence of molecular hydrogen. Applying an in situ formed ruthenium/triphos complex and an organic acid as cocatalyst, a broad range of alkylated secondary and tertiary amines are obtained in good to excellent yields. This novel method is also successfully applied for the synthesis of unsymmetrically substituted N-methyl/alkyl anilines through a direct three-component coupling reaction of the corresponding amines, carboxylic acids, and CO2 as a C1 source.
