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432-04-2

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432-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 432-04-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,3 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 432-04:
(5*4)+(4*3)+(3*2)+(2*0)+(1*4)=42
42 % 10 = 2
So 432-04-2 is a valid CAS Registry Number.
InChI:InChI=1/C3F9P/c4-1(5,6)13(2(7,8)9)3(10,11)12

432-04-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name tris(trifluoromethyl)phosphane

1.2 Other means of identification

Product number -
Other names Phosphine, tris(trifluoromethyl)-

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:432-04-2 SDS

432-04-2Relevant articles and documents

Facile syntheses of tris(trifluoromethyl) phosphine and difluorotris(trifluoromethyl)phosphorane

Goerg, Michaela,Roeschenthalera, Gerd-Volker,Kolomeitsev, Alexander A.

, p. 103 - 104 (1996)

Tris(trifluorornethyl)phosphine is easily available in high yield using the three component system P(NEt)2)3/CF3Br/(PhO)3P in HMPA. Addition of chlorine and fluorination with zinc difluoride yield difluorotris(trifluoromethyl)phosphorane.

Inorganic chemistry of fluorocarbenes. 1. Reactions of tetrafluoroethylidene with fluorine-containing phosphines

Sharp, Kenneth G.,Schwager, Irving

, p. 1697 - 1701 (2007/10/13)

The interactions of tetrafluoroethylidene with three fluorine-containing phosphines have been investigated. The source of the carbene is the pyrolytic decomposition of C2F5SiF3 at 200°C. The reaction of CF3CF with PF3 generates CF2=CFPF4 and PF5; reaction with (CF3)3P leads to (CF3)2PCF(CF3)2; and reaction with (CF3)2PCF(CF3)2 produces the fluorocarbon (CF3)2CFCF(CF3)2. The possibility that the vinylphosphorane product of the PF3 reaction results from fluorine-transfer rearrangement of C2F5PF2 as an intermediate product was discredited by a demonstration that C2F5PF2 is thermally stable under the reaction conditions. Other mechanistic pathways are discussed.

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