246257-66-9

Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
N-Benzyl-N-cyclopropylformamide is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals for its ability to contribute to the development of new therapeutic agents and pesticides.
Used in Cancer and Autoimmune Disorder Treatment:
BCF is used as a potential candidate for the treatment of various diseases, including cancer and autoimmune disorders, due to its unique chemical structure and potential therapeutic effects.
Used in Fragrance and Flavor Production:
N-Benzyl-N-cyclopropylformamide is used in the production of fragrances and flavors, capitalizing on its aromatic properties to create unique scents and tastes.
It is crucial to handle BCF with care, as it may pose health and environmental risks if not properly managed.

Upstream product

• 58644-54-5 N-cyclopropylformamide 
• 100-39-0 benzyl bromide 

Downstream Products

• 246257-67-0 benzyl-N,N-dicyclopropylamine 

Relevant academic research and scientific papers

TRIAZOLONES DERIVATIVES FOR USE IN THE TREATMENT, AMELIORATION OR PREVENTION OF A VIRAL DISEASE

The present invention relates to a compound having the general formula (I), optionally in the form of a pharmaceutically acceptable salt, solvate, polymorph, prodrug, tautomer, racemate, codrug, cocrystal, enantiomer, or diastereomer or mixture thereof, which is useful in treating, ameloriating or preventing a viral disease. Furthermore, specific combination therapies are disclosed.

Radical cations of trialkylamines: ESR spectra and structures

Novel syntheses of cyclopropyldiisopropylamine (15), di-tert- butylcyclopropylamine (16), dicyclopropylisopropylamine (17), and tricyclopropylamine (18) are described. Hyperfine data were determined by ESR spectroscopy for the radical cations of these trialkylamines, as well as for those of ethyldiisopropylamine (10), diisopropyl-n-propylamine (11), dicyclohexylethylamine (12), diisopropyl-3-pentylamine (14), and 1- azabicyclo[3.3.3]undecane (manxine; 27). The radical cation of triisopropylamine (13) was reexamined under conditions of improved spectral resolution. Coupling constants of the 14N nucleus and the β-protons in the radical cations of 18 trialkylamines provide reliable information about the geometries of these species, which are confirmed by theoretical calculations. With the exception of a few oligocyclic amines, for which flattening is impaired by the rigid molecular framework, all of the radical cations should be planar. Correlation between the observed coupling constants of the β- protons and the calculated 2 θ> values of the dihedral angle θ, defining the conformation of the alkyl substituent or the azacycloalkane, is verified. Upon oxidation, striking changes occur for those amines that have cyclopropyl substituents, because of the tendency of these groups to assume a perpendicular conformation in the neutral amines and a bisected orientation in the corresponding radical cations.