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112981-12-1

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112981-12-1 Usage

Description

Phosphorimidic triamide, N,N',N'',N'''-tetraphenyl-, also known as tetraphenyl phosphorimidic triamide, is a chemical compound with the molecular formula (C6H5)4P(NH)3. It is a phosphorimidic triamide that contains three nitrogen atoms and four phenyl groups bonded to a central phosphorus atom. Phosphorimidic triamide, N,N',N'',N'''-tetraphenylis known for its versatile properties and reactivity, making it of interest in various fields, including chemical research and industrial applications.

Uses

Used in Coordination Chemistry:
Phosphorimidic triamide, N,N',N'',N'''-tetraphenylis used as a ligand in coordination chemistry for the formation of metal complexes. Its ability to bind with metal ions allows it to play a crucial role in the synthesis and stabilization of various metal complexes.
Used in Catalysts:
Phosphorimidic triamide, N,N',N'',N'''-tetraphenylhas been studied for its potential applications in catalysis. Its unique structure and reactivity make it a promising candidate for use in catalytic processes, where it can facilitate chemical reactions and improve their efficiency.
Used in Organic and Inorganic Compounds Preparation:
Phosphorimidic triamide, N,N',N'',N'''-tetraphenylserves as a building block for the preparation of diverse organic and inorganic compounds. Its versatile properties enable it to be incorporated into a wide range of chemical structures, contributing to the development of new materials and compounds with various applications.
Used in Chemical Research:
Due to its unique structure and reactivity, this compound is of interest in chemical research. It can be used as a model compound to study the properties and behavior of phosphorimidic triamides, as well as to explore new synthetic routes and reaction mechanisms.
Used in Industrial Applications:
Phosphorimidic triamide, N,N',N'',N'''-tetraphenylhas potential applications in various industries, including pharmaceuticals, materials science, and chemical manufacturing. Its versatility and reactivity make it a valuable component in the development of new products and processes.

Check Digit Verification of cas no

The CAS Registry Mumber 112981-12-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,9,8 and 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 112981-12:
(8*1)+(7*1)+(6*2)+(5*9)+(4*8)+(3*1)+(2*1)+(1*2)=111
111 % 10 = 1
So 112981-12-1 is a valid CAS Registry Number.

112981-12-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[dianilino(phenylimino)-λ<sup>5</sup>-phosphanyl]aniline

1.2 Other means of identification

Product number -
Other names T0401-0158

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:112981-12-1 SDS

112981-12-1Relevant articles and documents

Organoamino phosphonium cations as building blocks for hierarchical supramolecular assemblies

Gupta, Arvind K.,Nicholls, Jennifer,Debnath, Suman,Rosbottom, Ian,Steiner, Alexander,Boomishankar, Ramamoorthy

scheme or table, p. 555 - 564 (2012/03/09)

Organoamino phosphonium cations of formula [P(NHR)4]+ offer four hydrogen bonding sites that are arranged in tetrahedral fashion around the central phosphorus atom. This arrangement generates novel supramolecular building blocks that are distinct from the commonly planar NH donor systems, such as urea and guanidine. The supramolecular aggregation of these cations in the presence of chloride and several carboxylate anions is described. The carboxylate salts are obtained either by anion exchange reactions with phosphonium chlorides or by protonation reaction of the neutral phosphine imine P(NPh)-(NHPh)3. X-ray structure analyses of the title compounds show that they form hierarchical structures ranging from 1D chains to 2D sheets and 3D networks. Control over the dimensionality of the supramolecular structure can be achieved by modulating the steric bulk of the phosphonium cation.

TETRAKIS(ALKYL- AND ARYLAMIDO)PHOSPHONIUM IODIDES

Kostina, V. G.,Rutkovskii, E. K.,Feshchenko, N. G.

, p. 955 - 960 (2007/10/02)

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