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(1R)-N-1-[3-(trifluoromethyl)phenyl]ethylmethylamine is a chiral amine compound characterized by a molecular formula of C11H14F3N. It features a tertiary amine group and a trifluoromethyl substituted phenyl group, which contribute to its unique structural and functional properties. (1R)-N-1-[3-(trifluoromethyl)phenyl]ethylmethylamine is recognized for its potential in both chemical and pharmaceutical research due to its versatile nature and the presence of distinct functional groups.

1212101-09-1

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1212101-09-1 Usage

Uses

Used in Pharmaceutical Industry:
(1R)-N-1-[3-(trifluoromethyl)phenyl]ethylmethylamine is utilized as a building block in organic synthesis, specifically within the pharmaceutical sector. Its unique structure allows it to be incorporated into the development of various drug compounds, enhancing the range of therapeutic options available.
Used as a Reagent in Chemical Reactions:
(1R)-N-1-[3-(trifluoromethyl)phenyl]ethylmethylamine also serves as a reagent in chemical reactions, facilitating specific transformations and syntheses. Its presence can influence the course of reactions, making it a valuable tool in the synthesis of complex organic molecules.
Used as a Ligand in Catalysis:
Furthermore, (1R)-N-1-[3-(trifluoromethyl)phenyl]ethylmethylamine functions as a ligand in catalysis. Its ability to bind to metal centers and influence the catalytic activity makes it a useful component in the design of catalysts for various chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 1212101-09-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,2,1,0 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1212101-09:
(9*1)+(8*2)+(7*1)+(6*2)+(5*1)+(4*0)+(3*1)+(2*0)+(1*9)=61
61 % 10 = 1
So 1212101-09-1 is a valid CAS Registry Number.

1212101-09-1Downstream Products

1212101-09-1Relevant articles and documents

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.

BENZIMIDAZOLYL-ACETAMIDE DERIVATIVES USEFUL AS POTASSIUM CHANNEL MODULATORS

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Page/Page column 22, (2013/07/25)

This invention relates to novel benzimidazolyl-acetamide derivatives to formula (l) and their use as modulators of small-conductance calcium-activated potassium channels (SK channels). Moreover the invention is directed to pharmaceutical compositions useful for the treatment or alleviation of diseases or disorders associated with the activity of potassium channels.

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