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2,2,4,4,6,6-hexakis(3,5-dimethyl-1H-pyrazol-1-yl)-1,3,5,2lambda~5~,4lambda~5~,6lambda~5~-triazatriphosphinine is a complex chemical compound characterized by its unique molecular structure. It consists of a triazatriphosphinine backbone to which six 3,5-dimethyl-1H-pyrazol-1-yl groups are attached. 2,2,4,4,6,6-hexakis(3,5-dimethyl-1H-pyrazol-1-yl)-1,3,5,2lambda~5~,4lambda~5~,6lambda~5~-triazatriphosphinine is known for its ability to form stable coordination complexes with a variety of metal ions, making it a versatile ligand in coordination chemistry.

74299-68-6

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74299-68-6 Usage

Uses

Used in Coordination Chemistry:
2,2,4,4,6,6-hexakis(3,5-dimethyl-1H-pyrazol-1-yl)-1,3,5,2lambda~5~,4lambda~5~,6lambda~5~-triazatriphosphinine is used as a ligand for forming coordination complexes with metal ions. Its structure allows it to act as a central atom, binding and stabilizing metal ions effectively.
Used in Catalysis:
2,2,4,4,6,6-hexakis(3,5-dimethyl-1H-pyrazol-1-yl)-1,3,5,2lambda~5~,4lambda~5~,6lambda~5~-triazatriphosphinine is utilized in catalysis due to its ability to form stable complexes with metal ions, which can enhance the efficiency of various chemical reactions.
Used in Chemical Synthesis:
2,2,4,4,6,6-hexakis(3,5-dimethyl-1H-pyrazol-1-yl)-1,3,5,2lambda~5~,4lambda~5~,6lambda~5~-triazatriphosphinine serves as a building block for the synthesis of more complex chemical compounds, contributing to the development of novel materials and molecules in the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 74299-68-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,2,9 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 74299-68:
(7*7)+(6*4)+(5*2)+(4*9)+(3*9)+(2*6)+(1*8)=166
166 % 10 = 6
So 74299-68-6 is a valid CAS Registry Number.

74299-68-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,4,4,6,6-hexakis(3,5-dimethylpyrazol-1-yl)-1,3,5-triaza-2λ<sup>5</sup>,4λ<sup>5</sup>,6λ<sup>5</sup>-triphosphacyclohexa-1,3,5-triene

1.2 Other means of identification

Product number -
Other names hexakis(3,5-dimethylpyrazolyl)cyclotriphosphazene

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:74299-68-6 SDS

74299-68-6Upstream product

74299-68-6Downstream Products

74299-68-6Relevant academic research and scientific papers

1-Pyrazolyl phosphazanes and their complexes with palladium(II) chloride and platinum(II) chloride

Gallicano, Keith D.,Paddock, Norman L.

, p. 521 - 528 (2007/10/02)

The chlorophosphazenes (NPCl2)3-6 and the phenylchlorophosphazenes gem-N3P3Ph4Cl2 and gem-N3P3Ph2Cl4 react with pyrazole, 3-methylpyrazole, and 3,5-dimethylpyrazole to give (NPpz2)3-6, 3-5, 3,4, N3P3Ph4(Mepz)2, N3P3Ph4(Me2pz)2, and N3P3Ph2(Me2pz)4.Infrared and nmr spectroscopy show the pyrazolyl group to be an electron-withdrawing substituent on the phosphazene ring, resembling a halogen rather than an amino group.The pyrazolyl group also acts as a donor through its pyridinic nitrogen atom, both intramolecularly and in the formation of thecomplexes gem-N3P3Ph4(Me2pz)2*PdCl2, gem-N3P3Ph2(Me2pz)4*PdCl2, N3P3(Me2pz)6*2PdCl2, N3P3(Me2pz)6*2PtCl2, and N3P3(Me2pz)6*3PdCl2.No bonding between the metal and a nitrogen atom in the ring was detected.

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