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N-(diphenylmethylene)octan-1-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51411-33-7

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51411-33-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51411-33-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,4,1 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51411-33:
(7*5)+(6*1)+(5*4)+(4*1)+(3*1)+(2*3)+(1*3)=77
77 % 10 = 7
So 51411-33-7 is a valid CAS Registry Number.

51411-33-7Downstream Products

51411-33-7Relevant academic research and scientific papers

Bidentate geometry-constrained iminopyridyl nickel-catalyzed synthesis of amines or imines via borrowing hydrogen or dehydrogenative condensation

Jiang, Yong,Hu, Miao,Sun, Nan,Hu, Baoxiang,Shen, Zhenlu,Hu, Xinquan,Jin, Liqun

supporting information, (2020/11/27)

The efficient Ni-catalyzed N-alkylation of various anilines with alcohols via borrowing hydrogen is reported using a bidentate geometry-constrained iminopyridyl nickel complex as the catalyst. Substituted benzylic alcohols and short/long chain aliphatic alcohols could be applied as the alkylation sources to couple with aromatic and heteroaromatic amines to give a diverse set of N-alkylation outcomes in moderate to excellent yields. The nickel catalytic system was also suitable for aliphatic amines, selectively delivering the corresponding imines via an acceptorless dehydrogenative condensation strategy.

Taking the F out of FLP: Simple lewis acid-base pairs for mild reductions with neutral boranes via borenium ion catalysis

Eisenberger, Patrick,Bailey, Adrian M.,Crudden, Cathleen M.

supporting information, p. 17384 - 17387 (2013/01/15)

Discrete three-coordinate borenium salts 1c and 1d are accessed by cooperative Lewis acid-base pair-mediated heterolytic splitting of the B-H bond in pinacolborane by B(C6F5)3DABCO and Ph 3C+/DABCO, respectively. The resulting salts are competent catalysts in the reduction of a broad range of imines and can be generated in situ. Moreover, a mechanistic framework for borenium catalysis based on experimental evidence is proposed. The reaction is suggested to proceed by borenium activation of the imine substrate followed by counterintuitive hydride delivery from HBPin (with the assistance of DABCO) rather than from the HB(C6F5)3- anion, contrary to typical mechanisms of reduction in FLP systems.

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