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Phosphine, (4-nitrophenyl)diphenyl-, also known as 4-nitrophenyl diphenyl phosphine, is an organophosphorus compound with the chemical formula C18H14NO2P. It is a yellow crystalline solid that is soluble in organic solvents such as ethanol and dichloromethane. Phosphine, (4-nitrophenyl)diphenyl- is primarily used as a reagent in organic synthesis, particularly in the preparation of various phosphorus-containing compounds and as a ligand in coordination chemistry. Due to its reactivity and potential toxicity, it is important to handle this chemical with care, following proper safety protocols.

5032-63-3

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5032-63-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5032-63-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,3 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5032-63:
(6*5)+(5*0)+(4*3)+(3*2)+(2*6)+(1*3)=63
63 % 10 = 3
So 5032-63-3 is a valid CAS Registry Number.

5032-63-3SDS

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 O-4-Nitrophenyl diphenylphosphinate

1.2 Other means of identification

Product number -
Other names Diphenyl-(4-nitro-phenyl)-phosphin

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:5032-63-3 SDS

5032-63-3Downstream Products

5032-63-3Relevant academic research and scientific papers

A practical synthesis of unsymmetrical triarylphosphines by heterogeneous palladium(0)-catalyzed cross-coupling of aryl iodides with diphenylphosphine

Xu, Zhaotao,Wang, Pingping,Chen, Qiurong,Cai, Mingzhong

, p. 50 - 58 (2018/04/23)

The heterogeneous cross-coupling reaction of aryl iodides with diphenylphosphine was achieved in DMAc at 130 °C in the presence of 1.0 mol% of MCM-41-supported tridentate nitrogen palladium(0) complex [MCM-41-3N-Pd(0)] with KOAc as base, yielding a variety of unsymmetrical triarylphosphines in good to excellent yields. The turnover frequency (TOF) of the catalyst can reach 30.67 h?1. This new heterogeneous palladium(0) catalyst could easily be prepared by a simple procedure from commercially readily available reagents, and exhibited the same catalytic activity as homogeneous Pd(OAc)2 or Pd(PPh3)4, and could be recovered by filtration of the reaction solution and recycled at least seven times without significant loss of catalytic activity.

An efficient heterogeneous cross-coupling of aryl iodides with diphenylphosphine catalyzed by copper (I) immobilized in MCM-41

Fang, Zhiqiang,Cai, Mingzhong,Lin, Yang,Zhao, Hong

, (2018/07/31)

The heterogeneous cross-coupling reaction of aryl iodides with diphenylphosphine was achieved in toluene at 115?°C in the presence of 10?mol% of phenanthroline-functionalized MCM-41-supported copper (I) complex (Phen-MCM-41-CuI) with Cs2CO3 as base, yielding various unsymmetric triarylphosphines in good to excellent yields. This protocol can tolerate a wide range of functional groups and does not need the use of expensive additives or harsh reaction conditions. This heterogeneous Cu (I) catalyst exhibited the same catalytic activity as homogeneous CuI/Phen system, and could easily be recovered by a simple filtration of the reaction solution and recycled up to seven times without significant loss of activity.

Ligand-free palladium catalyzed phosphorylation of aryl iodides

Nowrouzi, Najmeh,Keshtgar, Saba,Bahman Jahromi, Enayatollah

, p. 348 - 350 (2016/01/12)

A reusable ligand-free palladium catalyzed phosphorylation of aryl iodides using PdCl2/tetrabutylammonium bromide is described. Functionalized triarylphosphines were obtained in good to excellent yields in the absence of external reductants and supporting ligands.

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