1212124-79-2 Usage
Uses
Used in Pharmaceutical Industry:
(R)-N-[1-(3-Fluorophenyl)ethyl]methylamine is used as an intermediate in the synthesis of pharmaceutical compounds for the treatment of neurological and psychiatric disorders. Its unique structure allows for the development of potential drug candidates that can target specific receptors or pathways involved in these conditions, offering new therapeutic options for patients.
Used in Agrochemical Industry:
In the agrochemical industry, (R)-N-[1-(3-Fluorophenyl)ethyl]methylamine is utilized as a building block for the development of new agrochemicals. Its incorporation into the molecular structure of these chemicals can enhance their effectiveness in pest control, crop protection, and other agricultural applications, contributing to increased crop yields and more sustainable farming practices.
Used in Fine Chemicals Industry:
(R)-N-[1-(3-Fluorophenyl)ethyl]methylamine also finds application in the synthesis of specialty chemicals, which are used in various industries such as cosmetics, fragrances, and flavorings. Its unique properties enable the creation of novel compounds with specific functionalities, expanding the range of products available in these markets and potentially leading to innovative applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1212124-79-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,2,1,2 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1212124-79:
(9*1)+(8*2)+(7*1)+(6*2)+(5*1)+(4*2)+(3*4)+(2*7)+(1*9)=92
92 % 10 = 2
So 1212124-79-2 is a valid CAS Registry Number.
1212124-79-2Relevant academic research and scientific papers
Tackling N-Alkyl Imines with 3d Metal Catalysis: Highly Enantioselective Iron-Catalyzed Synthesis of α-Chiral Amines
Blasius, Clemens K.,Gade, Lutz H.,Heinrich, Niklas F.,Vasilenko, Vladislav
, p. 15974 - 15977 (2020/07/04)
A readily activated iron alkyl precatalyst effectively catalyzes the highly enantioselective hydroboration of N-alkyl imines. Employing a chiral bis(oxazolinylmethylidene)isoindoline pincer ligand, the asymmetric reduction of various acyclic N-alkyl imines provided the corresponding α-chiral amines in excellent yields and with up to >99 % ee. The applicability of this base metal catalytic system was further demonstrated with the synthesis of the pharmaceuticals Fendiline and Tecalcet.
