132951-64-5 Usage
Description
(1S)-1-(6-Methoxy(2-naphthyl))ethylamine is a chemical compound that belongs to the class of alkaloids. It is a substituted phenethylamine derivative with a molecular formula of C13H15NO and a molecular weight of 201.26 g/mol. (1S)-1-(6-METHOXY(2-NAPHTHYL))ETHYLAMINE is also known by its CAS number 59002-94-3. Its structure consists of a central amine group attached to a 2-naphthyl ring with an additional methoxy group and an ethyl chain.
Uses
Used in Organic Synthesis:
(1S)-1-(6-Methoxy(2-naphthyl))ethylamine is used as a building block in organic synthesis for the creation of various complex organic molecules. Its unique structure allows for versatile chemical reactions and the formation of a wide range of compounds.
Used in Pharmaceutical Research:
(1S)-1-(6-Methoxy(2-naphthyl))ethylamine is used as a starting material or intermediate in the development of new pharmaceuticals. Its structural features make it a promising candidate for the synthesis of potential drug molecules with novel biological activities and pharmacological properties.
Used in Biological Activity Studies:
(1S)-1-(6-Methoxy(2-naphthyl))ethylamine is used in biological activity studies to explore its potential as a bioactive compound. Further research is required to fully understand its potential uses and applications in various therapeutic areas.
Check Digit Verification of cas no
The CAS Registry Mumber 132951-64-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,9,5 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 132951-64:
(8*1)+(7*3)+(6*2)+(5*9)+(4*5)+(3*1)+(2*6)+(1*4)=125
125 % 10 = 5
So 132951-64-5 is a valid CAS Registry Number.
132951-64-5Relevant articles and documents
Synthesis of enantiopure 6-methoxy-2-naphthylglycolic acid and its application as a resolving agent
Shimada, Takayoshi,Kobayashi, Yuka,Saigo, Kazuhiko
, p. 3807 - 3813 (2007/10/03)
6-Methoxy-2-naphthylglycolic acid (6-MNGA) was designed as a novel acidic resolving agent, on the model of 2-naphthylglycolic acid (2-NGA). Enantiopure 6-MNGA was easily obtained from commercially available 2-bromo-6- methoxynaphthalene through four steps and was found to show a better chiral recognition ability for racemic 1-arylethylamines than the prototype 2-NGA did. The X-ray crystallographic analyses of less-soluble diastereomeric salts revealed that the introduction of a methoxy group at the 6-position of the 2-NGA skeleton made CH/π interaction(s) effective between 6-MNGA molecules and also between the 6-MNGA molecule and the target amine molecule. The methoxy group was also found to contribute to the realization of effective van der Waals interaction. These interactions played important roles for the stabilization of the less-soluble diastereomeric salts to improve the chiral recognition ability of 6-MNGA, compared to that of 2-NGA.
