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The chemical "N~2~,N~2~,N~4~,N~4~,N~6~,N~6~-hexamethyl-1,3,5,2lambda~5~,4lambda~5~,6lambda~5~-triazatriphosphinine-2,2,4,4,6,6-hexamine" is a complex organic compound with a unique structure. It consists of a triazatriphosphinine core, which is a heterocyclic compound containing three nitrogen atoms and one phosphorus atom. The compound is further characterized by the presence of six methyl groups (CH~3~) attached to the nitrogen atoms, and six additional nitrogen atoms forming the hexamine part of the molecule. The compound's structure is stabilized by the presence of three lambda~5~ bonds, which are a type of bond involving the overlap of a phosphorus atom's empty p-orbital with a nitrogen atom's lone pair of electrons. N~2~,N~2~,N~4~,N~4~,N~6~,N~6~-hexamethyl-1,3,5,2lambda~5~,4lambda~5~,6lambda~5~-triazatriphosphinine-2,2,4,4,6,6-hexamine is likely to have interesting properties due to its unique arrangement of atoms and bonds, and it may be of interest in the fields of organic chemistry, materials science, and potentially as a ligand in coordination chemistry.

1635-63-8

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1635-63-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1635-63-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,3 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1635-63:
(6*1)+(5*6)+(4*3)+(3*5)+(2*6)+(1*3)=78
78 % 10 = 8
So 1635-63-8 is a valid CAS Registry Number.

1635-63-8SDS

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 2-N,2-N',4-N,4-N',6-N,6-N'-hexamethyl-1,3,5-triaza-2λ<sup>5</sup>,4λ<sup>5</sup>,6λ<sup>5</sup>-triphosphacyclohexa-1,3,5-triene-2,2,4,4,6,6-hexamine

1.2 Other means of identification

Product number -
Other names Hexa(methylamino)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:1635-63-8 SDS

1635-63-8Downstream Products

1635-63-8Relevant academic research and scientific papers

Supramolecular variations on a molecular theme: The structural diversity of phosphazenes (RNH)6P3N3 in the solid state

Bickley, Jamie F.,Bonar-Law, Richard,Lawson, Gavin T.,Richards, Philip I.,Rivals, Frederic,Steiner, Alexander,Zacchini, Stefano

, p. 1235 - 1244 (2007/10/03)

Herein, we introduce an extremely 'soft' tecton, which interacts via 'soft' synthons displaying an unprecedented variety of supramolecular architectures in the solid state. Hexakis(organoamino) cyclotriphosphazene derivatives, (RNH)6P3/su

Synthesis and hydrolysis of hexakis(imidazolyl)cyclotriphosphazene

Allcock,Fuller

, p. 2250 - 2256 (2007/10/02)

The reaction of imidazole with hexachlorocyclotriphosphazene (I) has yielded hexakis(imidazolyl)cyclotriphosphazene (II). Compound II has been studied as a model for the analogous linear high polymer which is a prospective biodegradable carrier macromolecule. Compound II is hydrolytically unstable and decomposes to hydroxyphosphazenes, imidazole, and phosphate in aqueous media. A kinetic analysis of the removal of the first imidazolyl group from II in unbuffered 20% aqueous tetrahydrofuran within the pH range of 6.5-7.8 has shown that the hydrolysis is autocatalyzed by the free imidazole liberated in this step. Initially, the displacement of imidazole is a first-order process with respect to [II], but the release of imidazole gives rise to faster, second-order reaction in which the rate depends on the first powers of [II] and [imidazole]. The evidence favors the influence of free imidazole as a general-base catalyst and not via the formation of hydroxide ion. N-Methylimidazole reacts with I to form an unusual series of highly reactive yellow salts of the general formula [N3P3Cl6-x(C4H6N 2)x]x+XCl (VII). The chemistry of II and VII is discussed in terms of its relationship to the synthesis and reactions of the analogous linear high polymeric phosphazenes.

Positional and cis-trans N-methylaminotriphosphonitriles. The use of H1 nuclear magnetic resonance in configurational analysis

Ford,Dickson,Bezman

, p. 890 - 893 (2007/10/05)

Through aminolysis with methylamine, phenylation with benzene in the presence of aluminum chloride, and a combination of both, a series of derivatives of trimeric phosphonitrilic chloride has been made. H1 nuclear magnetic resonance spectra were obtained for these compounds and used to determine both their positional and cis-trans configurations. The structural analysis is based on consideration of the number of chemical environments and the values of the coupling constants.

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