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Pentamethylpentaphospholane, also known as (Me5P4), is a phosphorus-containing organometallic compound with the chemical formula C5H15P5. It is a cyclic molecule consisting of a pentagonal phosphorus ring with each phosphorus atom bonded to a methyl group (CH3). pentamethylpentaphospholane is a colorless, volatile, and highly flammable liquid with a pungent odor. Pentamethylpentaphospholane is an important ligand in organophosphorus chemistry, used in the synthesis of various phosphorus-containing compounds and as a precursor in the production of other organophosphorus compounds. It is also known for its potential applications in catalysis and as a flame retardant. Due to its highly reactive nature, it requires careful handling and storage.

1073-98-9

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1073-98-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1073-98-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1073-98:
(6*1)+(5*0)+(4*7)+(3*3)+(2*9)+(1*8)=69
69 % 10 = 9
So 1073-98-9 is a valid CAS Registry Number.

1073-98-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,4,5-pentamethylpentaphospholane

1.2 Other means of identification

Product number -
Other names Pentamethyl-cyclopentaphosphan

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:1073-98-9 SDS

1073-98-9Downstream Products

1073-98-9Relevant academic research and scientific papers

Ylidylphosphanes and -diphosphanes

Breitsameter, Florian,Schmidpeter, Alfred,Schier, Annette

, p. 381 - 388 (2007/10/03)

Chlorophosphanyl and dichlorophosphanyl alkylidene- and benzylidenephosphoranes 6 and 8 are converted by reaction with LiAlH4 to the respective phosphanes 7 and 9. The former can be isolated, but decompose on heating or on protonation to give the ylidyl diphosphane 11 and the phosphonium ylide or phosphonium salt, respectively. The final products are the cyclooligophosphanes 15-17. Only the C-tert-butyl derivative 7c is stable in both regards. The conformation of the RPH group in 7 as compared to that of the RPCl group in 6 clearly reflects their different interaction with the ylide moiety.

OBERFLAECHEN-REAKTIONEN 15 Heterogene Dechlorierungen von Phosphorchloriden (X)PCl3 und R-PCl2 an , , x/TiO2> und sowie spektroskopische Evidenz fuer das Entstehen von Diphospha-dicyan PC-CP aus Cl2P-CC-PCl2

Bock, H.,Bankmann, M.

, p. 167 - 191 (2007/10/02)

Stimulated by the successful generation of unsaturated molecules with low-coordinated phosphorus centers by heterogeneous surface dechlorination, Cl2P-CC-PCl2 is synthesized and characterized by PE and mass spectra.In addition, curls, wool and catalysts x/TiO2> or are tested as potential dechlorinating agents for phosphorus halides like OPCl3, SPCl3, H3C-PCl2, H5C2-PCl2, (H3C)3C-PCl2 or H5C6-PCl2 in a gasflow reactor under reduced pressure and yield, inter alia, the following representative results: due to the thermodynamically favored formation of , or at the Mg surface, P4 is the only gaseous product identified from reactions of OPCl3 and SPCl3 with metal at higher temperatures.On the contrary, passing H3C-PCl2 at 600K over yields a reaction mixture containing P(CH3)3, (H3C)2P-P(CH3)2 (H3C-P)5 and CH4, which suggests an intermediate formation of surface phosphinidenes Mg>.Analogously, the pentamer (H3C-H2C-P)5 can be isolated from ethyldichlorophosphane.Reaction of the evaporated diphospha-cyanogen precursor Cl2P-C-PCl2 with the catalyst produces predominantly PCl3, and P4, but PE and mass spectra provide evidence that also minor amounts of the hitherto unknown molecule PC-CP are formed.

Evidence for Surface Phosphinidene Intermediates Mg> in the Heterogeneous Dechlorination of Alkyldichlorophosphanes RPCl2 by Mg Metal

Bock, Hans,Bankmann, Martin

, p. 1130 - 1132 (2007/10/02)

The heterogeneous dechlorination of alkyldichlorophosphanes by Mg metal at 600 K yields chemisorbed products which include penta-alkylcyclopentaphosphanes (RP)5, in addition to RnPH(3-n), R2P-PR2, P4, RH, and R-R, and thus provides evidence for surface phosphinidene intermediates Mg>.

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