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Phosphenimidous amide, N,N'-diphenyl-, also known as N,N'-diphenylphosphenimidous amide, is an organophosphorus compound with the chemical formula C14H12NP. It is a colorless solid that is sensitive to air and moisture, and it is commonly used as a reagent in organic synthesis, particularly in the formation of phosphorus-nitrogen bonds. The compound is prepared by the reaction of diphenylphosphine with hydroxylamine, and it is known for its ability to act as a reducing agent, facilitating various chemical transformations. Due to its reactivity, it is typically handled under an inert atmosphere to prevent unwanted side reactions.

5679-59-4

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5679-59-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5679-59-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,7 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5679-59:
(6*5)+(5*6)+(4*7)+(3*9)+(2*5)+(1*9)=134
134 % 10 = 4
So 5679-59-4 is a valid CAS Registry Number.

5679-59-4SDS

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-phenyliminophosphanylaniline

1.2 Other means of identification

Product number -
Other names N-phenylphosphazoanilide

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:5679-59-4 SDS

5679-59-4Upstream product

5679-59-4Relevant academic research and scientific papers

Synthesis and properties of 1,2-dihydro-4(3H)-quinazolinones

Khachatryan,Belus,Misyurin,Baryshnikova,Kolotaev,Matevosyan

, p. 1044 - 1058 (2017/10/31)

We modified the preparative-scale method for the synthesis of 2-aryl 1,2-dihydro-4(3H)-quinazolinone derivatives obtained in high yields by the reaction of new and commercially available aromatic aldehydes with anthranilic acid amides. A series of quinazolinone derivatives possessing anticancer and antiparasitic activities, as well as capable of preventing the progress of neurodegenerative diseases were characterized. There are grounds for clinical trials of these substances in order to select compounds being promising for clinical application.

Novel approach for the synthesis of N-substituted-4-(2-methyl-4-oxo- 4hquinazolin- 3-YL)-butyramides

Amir, Mohammad,Ali, Israr

experimental part, p. 2086 - 2095 (2011/07/31)

A simple and convenient method for the synthesis of N-substituted-4-(2- methyl- 4-oxo-4H-quinazolin-3-yl)-butyramides has been reported. Several aromatic and aliphatic amide derivatives of 4-(2-methyl-4-oxo-4H-quinazolin-3- yl)-butyric acid were prepared

An efficient route to vinyl substituted oxadiazoles and triazoles using phenylselanyl derivatives as precursor

Wang, Yu-Guang,Huang, Xian,Wu, Yu-Zhou

, p. 7866 - 7873 (2008/02/08)

Vinyl substituted oxadiazoles and triazoles were obtained from selenoxide syn-elimination of phenylselanylethyl substituted oxadiazoles and triazoles, which were prepared through hydrazinolysis, acylation, and cyclocondensation reactions of phenylselanyl-

The phosphazo route to 2-alkenamides from acrylic acid and its derivatives

Cabral, Jose,Laszlo, Pierre,Montaufier, Marie-Therese,Lalatiana Randriamahefa

, p. 1705 - 1708 (2007/10/02)

2-Alkenamides are formed in good isolated yields (generally up to 70%) by the reaction of in situ-generated phosphazo compounds issued from aliphatic, alicyclic and aromatic primary amines, with acrylic acid and its derivatives.

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