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Benzenamine, N-[(2-iodophenyl)methylene]-4-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39087-86-0

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39087-86-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39087-86-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,0,8 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 39087-86:
(7*3)+(6*9)+(5*0)+(4*8)+(3*7)+(2*8)+(1*6)=150
150 % 10 = 0
So 39087-86-0 is a valid CAS Registry Number.

39087-86-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-iodobenzylidene)-4-methoxyaniline

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:39087-86-0 SDS

39087-86-0Relevant academic research and scientific papers

Ir-Catalyzed C?H Amidation of Aldehydes with Stoichiometric/Catalytic Directing Group

Zhang, Yun-Fei,Wu, Bin,Shi, Zhang-Jie

supporting information, p. 17808 - 17812 (2016/11/28)

Ir-catalyzed sp2C?H amidation of aldehydes with various anilines as stoichiometric or catalytic directing groups was accomplished. A wide range of substrates were selectively amidated in good to excellent yields with broad functional group tolerance. The iridacycle complexes were isolated, characterized, and proved as key intermediates. Kinetic studies and Hammett plots provided detailed understandings of this amidation. According to the mechanism, the electron-rich ArSO2N3was proved effective for intermolecular sp3C?H amidation.

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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