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1,3,5,2,4,6-Triazatriphosphorine, 2,2,4,4,6,6-hexakis(4-bromophenoxy)-2,2,4,4,6,6-hexahydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

4376-72-1

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4376-72-1 Usage

Composition

Contains phosphorus and bromine atoms

Reactivity

Highly reactive

Toxicity

Potentially toxic

Industrial Applications

Used in various industrial processes and research applications

Potential Applications

Flame retardants, pesticides, and as a building block for organic synthesis

Handling Precautions

Must be handled with caution due to potential hazards to human health and the environment

Structural Features

The compound has a triazatriphosphorine core with six bromophenoxy groups attached to the carbon atoms in the 2, 4, and 6 positions, and a hexahydro group attached to the 2, 2, 4, 4, 6, and 6 positions.

Check Digit Verification of cas no

The CAS Registry Mumber 4376-72-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,7 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4376-72:
(6*4)+(5*3)+(4*7)+(3*6)+(2*7)+(1*2)=101
101 % 10 = 1
So 4376-72-1 is a valid CAS Registry Number.

4376-72-1SDS

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 hexakis(p-bromophenoxy)cyclotriphosphazene

1.2 Other means of identification

Product number -
Other names Hexakis-[4-brom-phenoxy]-cyclotriphosphazatrien

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:4376-72-1 SDS

4376-72-1Relevant academic research and scientific papers

A POSS-Phosphazene Based Porous Material for Adsorption of Metal Ions from Water

Soldatov, Mikhail,Liu, Hongzhi

, p. 4345 - 4351 (2019)

The development of adsorptive materials continues to be an important area of research for removal of heavy metal ions from waste water. The adsorption capacity can be modulated by both physical and chemical modification of the adsorbent. Herein, we combin

Synthesis and characterization of new (dimethylsilyl)phenoxy and (dimethyl(vinyl)silyl)phenoxy substituted cyclotriphosphazenes

Januszewski, Rafa?,Dutkiewicz, Micha?,Kubicki, Maciej,Dutkiewicz, Grzegorz,Maciejewski, Hieronim,Marciniec, Bogdan

, p. 64 - 67 (2017)

The routes of synthesis, as well as, spectroscopic and X-ray diffraction characterization of a new group of bis- or hexakis-4-(dimethyl(vinyl)silyl)phenoxy and 4-(dimethylsilyl)phenoxy-substituted cyclotriphosphazenes as a versatile starting substrates for the synthesis of a variety of organic cyclophosphazene derivatives, via catalytic hydrosilylation or silylative coupling processes, is presented.

Pd complexes based on phosphine-linked cyclophosphazenes: Synthesis, characterization and application in suzuki coupling reactions

De Paula, Vanderlei I.,Sato, Cintia A.,Buffon, Regina

experimental part, p. 258 - 266 (2012/05/05)

Palladium complexes were obtained by reaction of phosphine-linked cyclophosphazenes, (P3N3)(O-C6H 4-PR2)6, where R = phenyl, i-propyl or cyclohexyl, with using a Pd/ligand molar ratio of 3/1. The (P3N 3)(O-C6H4-PR2)6Pd 3(dba)x complexes were characterized by elemental analyses, mass spectrometry, 31P NMR and FT-IR where a characteristic nC=C band of dba coordinated to palladium was always observed. All complexes were tested in Suzuki coupling reactions between phenylboronic acid and aryl halides. Turnover numbers as high as ca. 17,500 for the coupling of 2-bromotoluene with chlorophenylboronic acid could be obtained for R = cyclohexyl. The complex based on -PPh2 was also immobilized in silica matrixes by the sol-gel method. Preliminary experiments showed that the immobilized catalyst could be used in at least three consecutive Suzuki reactions with the same catalytic activity.

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