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(E)-1-(2-bromophenyl)-N-(1-phenylethyl)methanimine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

108791-86-2

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108791-86-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108791-86-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,7,9 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 108791-86:
(8*1)+(7*0)+(6*8)+(5*7)+(4*9)+(3*1)+(2*8)+(1*6)=152
152 % 10 = 2
So 108791-86-2 is a valid CAS Registry Number.

108791-86-2Downstream Products

108791-86-2Relevant academic research and scientific papers

O-Naphthoquinone-Catalyzed Aerobic Oxidation of Amines to (Ket)imines: A Modular Catalyst Approach

Goriya, Yogesh,Kim, Hun Young,Oh, Kyungsoo

, p. 5174 - 5177 (2016)

A modular aerobic oxidation of amines to imines has been achieved using an ortho-naphthoquinone (o-NQ) catalyst. The cooperative catalyst system of o-NQ and Cu(OAc)2 enabled the formation of homocoupled imines from benzylamines, while the presence of TFA helped the formation of cross-coupled imines in excellent yields. The current mild aerobic oxidation protocol could also be applied to the oxidation of secondary amines to imines or ketimines with the help of cocatalyst, Ag2CO3, with excellent yields.

Further Studies of the Kinetic Template Effect in the Metal Ion-catalysed Reactions of ortho-Donor-substituted Aryl Halides with Tertiary Phosphines. Structural Requirements of the Template

Allen, David W.,Cropper, Paul E.,Smithurst, Peter G.,Ashton, Peter R.,Taylor, Brian F.

, p. 1989 - 1994 (2007/10/02)

The reactions of a series of Schiff's bases, derived from ortho-chloro-, bromo- or iodo-benzaldehydes and p-anisidine, with tertiary phosphines in the presence of nickel(II) bromide in refluxing ethanol proceed with displacement of the ortho-halogen to form the related ortho-substituted arylphosphonium salts.These reactions appear to be examples of a kinetic template effect in which the Schiff's base moiety aids the catalytic role of the metal ion in promoting the substitution reaction.Introduction of a second donor atom into the substituent group present at the nitrogen of related Schiff's bases inhibits the reactions due to diversion of the metal ion in other modes of coordination.The reactions are also inhibited by steric crowding at the imino-nitrogen.A range of other aryl halides bearing ortho-substituents having the potential to act as co-ordination templates has been prepared and their reactions with phosphines in the presence of metal ions studied enabling the rather critical nature of effective template groups to be defined.Detailed 13C n.m.r. data are also reported for the Schiff's bases and related arylphosphonium salts.

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