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Tetraethylphosphonium chloride (TEPC) is a quaternary phosphonium salt with the chemical formula (C2H5)4P+Cl-. It is a colorless, viscous liquid that is soluble in water and organic solvents. TEPC is widely used as a phase-transfer catalyst in organic synthesis, facilitating the transfer of reactants between aqueous and organic phases. It is also employed as a flame retardant, corrosion inhibitor, and in the production of various phosphorus-containing compounds. Due to its potential health and environmental risks, proper handling and disposal procedures should be followed when working with TEPC.

7368-65-2

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7368-65-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7368-65-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,6 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7368-65:
(6*7)+(5*3)+(4*6)+(3*8)+(2*6)+(1*5)=122
122 % 10 = 2
So 7368-65-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H21P.ClH/c1-5-9(6-2,7-3)8-4;/h9H,5-8H2,1-4H3;1H

7368-65-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name tetraethylphosphanium,chloride

1.2 Other means of identification

Product number -
Other names Tetraaethyl-phosphonium,Tetraaethylphosphoniumchlorid

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:7368-65-2 SDS

7368-65-2Relevant academic research and scientific papers

Heteroorganic betaines 3. * Reactions of betaines containing the +P-C-Si-S- fragment

Borisova,Zemlyanskii,Shestakova,Khrustalev,Ustynyuk,Chernyshev

, p. 933 - 941 (2007/10/03)

The [Ph3P+-CMe2-SiMe2-SEt]Br- salt was prepared by the reaction of betaine Ph3P+-CMe2SiMeR-S- (1a: R = Me) with EtBr. Acetylation of betaine 1a or Et3P+-CHMeSiMe2-S- (2a) afforded 2,2,6-trimethyl-1,3-dioxa-2-silacyclohex-5-ene-4-thione Me2SiOC(=S)CH=C(Me)O or the [Et3P+-CHMeSiMe2Cl]Cl- salt depending on the reagent ratio. The reactions of betaines 1a,b (1b: R = Ph) or 2 with compounds (R3Sn)2X (X = O or NMe) can be used for the generation of silanones [RMeSi=O] and silaneimines [RMeSi=NMe] in solutions. The reactivity of betaines Ph3P+-CHR1SiMeR2-S- (R1 = H or Me and R2 = Me or Ph) is determined by the equilibrium between the zwitterionic and ylide Ph3P=CR1SiMeR2SH tautomers that exist in solutions.

Reaktion von Acetyl-Uebergangsmetallkomplexen mit Phosphor-Yliden - ein weiteres Beispiel zur Halogenid/Metallat-Analogie

Malisch, Wolfgang,Blau, Herbert,Haaf, Franz Jakob

, p. 2956 - 2970 (2007/10/02)

The reaction of the acetyl metal complexes LnM-C(O)CH3Mo> with the phosphorus ylides (CH3)3P=CH2, C2H5(CH3)2P=CH2, (C2H5)3P=CHCH3 and (C4H9)3P=CH2 in the ratio 1:2 yields the corresponding acetyl-substituted ylides R3P=CR'C(O)CH3 3a - d (R = CH3, C2H5, n-C4H9; R' = H, CH3) and phosphonium metalates 4a - d, 6a, b via heterolysis of the Fe-C-?-bond and transylidation.With CH3C(O)Cl an analogous way of reaction is observed, which however can be repeated to give the diacetyl ylides R3P=C(COCH3)2 8a, b (R = CH3, n-C4H9).The new compounds are characterized by spectroscopic methods (NMR, IR) and further reactions.

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