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Phosphinic amide, N-(diphenylmethyl)-P,P-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71847-25-1

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71847-25-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71847-25-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,8,4 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 71847-25:
(7*7)+(6*1)+(5*8)+(4*4)+(3*7)+(2*2)+(1*5)=141
141 % 10 = 1
So 71847-25-1 is a valid CAS Registry Number.

71847-25-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name P,P-diphenyl-N-(diphenylmethyl)phosphinic amide

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:71847-25-1 SDS

71847-25-1Relevant academic research and scientific papers

Copper-Catalyzed (Di)Arylmethylation of Phosphorylamides Under Oxidative Conditions

Zhao, Zijian,Liu, Xiaobo,Hou, Anguo,Lian, Yan

, p. 6857 - 6866 (2019/01/04)

A compatible and practical (di)arylmethylation of phosphorylamides was successfully accessed in the presence of copper iodide as the catalyst, azodiisobutyronitrile as the radical initiator, and di-tert-butyl peroxide as the oxidant. Both methylarenes and diaryl methanes were compatible under the oxidative conditions, enjoying broad functional groups tolerance (51 examples) and good efficiency (up to 90 % yields).

Cobalt-catalyzed oxidative arylmethylation of phosphorylamides

Xiao, Jing,Li, Ping,Zhang, Yingjun,Xie, Dexun,Peng, Zhihong,An, Delie,Dong, Wanrong

, p. 4558 - 4568 (2018/07/30)

A cobalt-catalyzed strategy for N-arylmethylation of phosphorylamides was herein achieved with the assistance of azodiisobutyronitrile as the radical initiator and di-tert-butyl peroxide as the oxidant. Both methylarenes and diaryl methanes were compatible under the oxidative conditions, expressing broad substrate scope (51 examples) and high efficiency (up to 87% yield).

Tertiary α-diarylmethylamines derived from diarylketimines and organomagnesium reagents

Desmarchelier, Alaric,Ortiz, Pablo,Harutyunyan, Syuzanna R.

, p. 703 - 706 (2015/01/09)

Organomagnesium reagents enable swift and versatile derivatisation of diarylimines to the corresponding α-substituted diarylmethylamines in excellent yields, through fast and clean reactions. Where it occurs, 1,2-reduction can be circumvented using readily accessible dialkylmagnesium reagents. This journal is

Synthesis and structural studies of dimeric sodium compounds having pentametallacyclooctane and hexametallacyclo undecane structure using different phosphinamine derivatives

Kottalanka, Ravi K.,Naktode, Kishor,Panda, Tarun K.

, p. 188 - 195 (2013/04/10)

The treatment of two bulky phosphinamines [Ph2PNH(CHPh 2)] (1) and [Ph2PNH(CPh3)] (2) with 30% hydrogen peroxide afforded phosphinicamides [Ph2P(O)NH(CHPh 2)] (3) and [Ph2P(O)NHC

Rh-N-heterocyclic carbene (NHC) complex-catalyzed addition of phenylboronie acid to N-sulfonyl and N-phosphinoyl aldimines

Md., Abu Bakar,Suzuki, Yumiko,Sato, Masayuki

experimental part, p. 973 - 976 (2009/07/18)

Rh-N-heterocyclic carbene (NHC) complexes were generated in situ from imidazolium salts, [RhCl(cod)]2 and t-BuOK in dioxane. In the presence of a catalytic amount of Rh-NHC complexes, the addition reaction of phenylboronic acid to N-sulfonylarylimines and N-phosphinyolarylimines gave the corresponding amines in high yields.

Nickel-catalysed addition of dialkylzinc reagents to N-phosphinoyl- and N-sulfonylimines

Almansa, Raquel,Guijarro, David,Yus, Miguel

, p. 1167 - 1174 (2007/10/03)

A catalytic amount of a nickel complex (0.1-5.3 mol %) extraordinarily increases the reaction rate of the addition of dialkylzinc reagents to N-(diphenylphosphinoyl)- or N-(benzenesulfonyl)imines. The reaction of imines derived from both aromatic and alip

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