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1-Benzyl-2,2,6,6-tetramethyl-piperidine is a complex organic compound with the molecular formula C18H29N. It is a derivative of piperidine, a cyclic amine, and features a benzyl group attached to the first carbon atom. The molecule also contains four methyl groups, which are attached to the second, sixth, and two additional carbon atoms. 1-benzyl-2,2,6,6-tetramethyl-piperidine is known for its potential applications in the synthesis of pharmaceuticals and other chemical products, particularly in the area of chiral ligands and catalysts. It is an important intermediate in the preparation of certain drugs and is also used in the production of some specialty chemicals. The compound's structure and properties make it a valuable component in various chemical reactions and processes.

783-76-6

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783-76-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 783-76-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,8 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 783-76:
(5*7)+(4*8)+(3*3)+(2*7)+(1*6)=96
96 % 10 = 6
So 783-76-6 is a valid CAS Registry Number.

783-76-6Downstream Products

783-76-6Relevant academic research and scientific papers

Metal-Free C?H Borylation of N-Heteroarenes by Boron Trifluoride

Iashin, Vladimir,Berta, Dénes,Chernichenko, Konstantin,Nieger, Martin,Moslova, Karina,Pápai, Imre,Repo, Timo

, p. 13873 - 13879 (2020)

Organoboron compounds are essential reagents in modern C?C coupling reactions. Their synthesis via catalytic C?H borylation by main group elements is emerging as a powerful tool alternative to transition metal based catalysis. Herein, a straightforward metal-free synthesis of aryldifluoroboranes from BF3 and heteroarenes is reported. The reaction is assisted by sterically hindered amines and catalytic amounts of thioureas. According to computational studies the reaction proceeds via frustrated Lewis pair (FLP) mechanism. The obtained aryldifluoroboranes are further stabilized against destructive protodeborylation by converting them to the corresponding air stable tetramethylammonium organotrifluoroborates.

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