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N-[2-(Diphenylphosphino)benzylidene]cyclohexylamine, 97% is a chemical compound with the molecular formula C27H24NP. It is a phosphine ligand, which is a type of ligand that can bind to metal centers in coordination complexes. N-[2-(Diphenylphosphino)benzylidene]cyclohexylamine, 97% is characterized by its high purity (97%) and is known for its potential applications in various chemical reactions and processes.

321155-13-9

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321155-13-9 Usage

Uses

1. Used in Catalyst Applications:
N-[2-(Diphenylphosphino)benzylidene]cyclohexylamine, 97% is used as a catalyst for cross-coupling reactions, which are essential in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and advanced materials.
2. Used in Stannylative Cycloaddition Applications:
In the field of organic chemistry, N-[2-(Diphenylphosphino)benzylidene]cyclohexylamine, 97% is used as a catalyst for stannylative cycloaddition of conjugated enynes. This reaction is significant for the formation of complex molecular structures with potential applications in the development of new drugs and materials.
3. Used in Stereoand Regioselective Alkynylstannylation Applications:
N-[2-(Diphenylphosphino)benzylidene]cyclohexylamine, 97% is also utilized as a catalyst for stereoand regioselective alkynylstannylation of alkynes. This reaction is crucial for the synthesis of specific isomers of organic compounds, which can have different properties and applications in various industries, such as pharmaceuticals and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 321155-13-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,1,1,5 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 321155-13:
(8*3)+(7*2)+(6*1)+(5*1)+(4*5)+(3*5)+(2*1)+(1*3)=89
89 % 10 = 9
So 321155-13-9 is a valid CAS Registry Number.

321155-13-9 Well-known Company Product Price

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  • Aldrich

  • (720038)  N-[2-(Diphenylphosphino)benzylidene]cyclohexylamine  97%

  • 321155-13-9

  • 720038-500MG

  • 1,297.53CNY

  • Detail

321155-13-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-N-Cyclohexyl-1-[2-(diphenylphosphino)phenyl]methanimine

1.2 Other means of identification

Product number -
Other names 2-(diphenylphosphanyl)-N-cyclohexyliminobenzaldehyde

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:321155-13-9 SDS

321155-13-9Relevant articles and documents

Rh(i) complexes supported on a biopolymer as recyclable and selective hydroformylation catalysts

Makhubela, Banothile C. E.,Jardine, Anwar,Smith, Gregory S.

experimental part, p. 338 - 347 (2012/04/10)

Chitosan-supported Rh complexes were prepared in a stable form to form new catalysts and have been characterized using elemental analysis, UV-vis, FT-IR, ICP-MS, PXRD, solid state 31P and 13C NMR spectroscopy and TEM. Mononuclear Rh(i) complexes (as models for the heterogenized catalysts) were also prepared via the Schiff-base condensation reaction and the crystal structure of the cyclohexyl iminophosphine Rh(i) complex was elucidated. The chitosan-supported Rh complexes and mononuclear analogues are active catalysts in the hydroformylation of 1-octene with optimal reaction conditions realized at 75 °C and 30 bar syngas pressure. Under these conditions, 1-octene conversion to the desired linear aldehydes was observed and the best selectivity in this regard was shown by the supported iminophosphine-based rhodium catalyst. Overall, the supported catalysts showed similar chemo- and regioselectivities in comparison to their mononuclear counterparts but where more stable, being reused up to four times without loss of activity and selectivity.

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