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Dimethyltrifluorophosphorane, also known as (MeO)PF3, is a colorless, volatile, and highly reactive organophosphorus compound with the chemical formula (CH3)2PF3. It is widely used as a reagent in the synthesis of various organophosphorus compounds, particularly in the preparation of phosphine oxides and phosphines. Due to its high reactivity, it is essential to handle dimethyltrifluorophosphorane with caution, as it can react violently with water and is sensitive to moisture. Additionally, it is toxic and has a pungent odor, necessitating proper safety measures during its use and storage.

811-79-0

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811-79-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 811-79-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,1 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 811-79:
(5*8)+(4*1)+(3*1)+(2*7)+(1*9)=70
70 % 10 = 0
So 811-79-0 is a valid CAS Registry Number.

811-79-0SDS

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 trifluoro(dimethyl)-λ<sup>5</sup>-phosphane

1.2 Other means of identification

Product number -
Other names Dimethyl-tri-fluorophosphoran

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:811-79-0 SDS

811-79-0Downstream Products

811-79-0Relevant articles and documents

Preparation and properties of dimethyltetrafluorophosphate

Hohenstein, Christian,Kornath, Andreas,Neumann, Frank,Ludwig, Ralf

body text, p. 6421 - 6427 (2010/10/21)

Dimethyltrifluorophosphorane reacts with strong fluoride donors, such as CsF, Me4NF, and Me4PF, under formation of dimethyltetrafluorophosphates. The salts were characterized by infrared and Raman spectroscopy and in acetonitrile solutions by NMR spectroscopy. The experimental results show that only the trans isomer is formed. Theoretical calculations (B3LYP/6-31 +G* and RHF/6-31 +G*) of the trans and cis isomer yielded a difference of the Gibbs free energy of 29.4 kJ/mol (B3LPY/6-31 +G*). The Me4N+[Me2PF4] - crystallizes in the orthorhombic space group Pnma with four formula units per unit cell and dimensions of a = 1303.5(3), b = 799.8(2), and c = 1023.8(4) pm. The phosphorus atom has an octahedral environment with P-C distances of 183.4(3) pm and P-F bond lengths in the range between 166.1(1) and 168.2(1) pm. In the crystal packing, anions and cations are linked via weak fluorine hydrogen contacts forming a three-dimensional network.

Perfluormethyl Element Ligands, XXIV; Organotin Compounds as Reagents, III. Cleavage Reactions of the Element-Element-Bond in Compounds of the Type RnE-ERm (R = CH3, CF3; E = P, As, S, Se, Te; n, m = 1, 2)

Dehnert, Peter,Grobe, Joseph,Van, Duc Le

, p. 48 - 54 (2007/10/02)

A systematic study of the cleavage of element-element bonds in compounds of the type RnE-ERm (R = CH3, CF3; E = P, As, S, Se, Te; n, m = 1, 2) by the group IV A element hydrides Me3M'H (M' = Si, Ge, Sn; Me = CH3) has been carried out.To evaluate the reaction pathway, for a number of compounds the attack of H2O, CH3OH, HBr and HI has been investigated.Possible reaction intermediates have been synthesized by independent routes and tested under comparable conditions. - Keywords: Organoelement-Element Compounds, Perfluoromethyl Derivatives, NMR Spectra

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