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14353-90-3

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14353-90-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14353-90-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,5 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14353-90:
(7*1)+(6*4)+(5*3)+(4*5)+(3*3)+(2*9)+(1*0)=93
93 % 10 = 3
So 14353-90-3 is a valid CAS Registry Number.

14353-90-3SDS

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 1,2,3,4,5-pentafluoro-6-iodosylbenzene

1.2 Other means of identification

Product number -
Other names PFIB

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:14353-90-3 SDS

14353-90-3Relevant articles and documents

Catalytic reactivity of a meso-N-substituted corrole and evidence for a high-valent iron-oxo species

McGown, Amanda J.,Kerber, William D.,Fujii, Hiroshi,Goldberg, David P.

experimental part, p. 8040 - 8048 (2009/12/02)

It is shown that an iron(III) meso-N-substituted corrole (TBP 8Cz)FeIII (1) (TBP8Cz = octakis(4-tert- butylphenyl)corrolazinato), is a potent catalyst for the oxidation of alkenes in the presence of pentaflouroiodosylbenzene (C6F5IO)as oxidant. In the case of cyclohexene, complex 1 performs on a par wit h one of the best porphyrin catalysts ((TPPF20)FeCl), exhibiting rapid turnover and a high selectivity for epoxide (CzFeIII/C6F 5IO/cyclohexene (1:100:1000) in CH2Cl2/CH 3OH (3:1 v:v) gives 33 turnovers of epoxide in max = 440, 611, 747 nm) under single-turnover-like conditions at -78°C leads to the formation of a new dark-brown species (2) (λmax = 396, 732, 843 nm). The FeIII complex 1 is restored upon the addition of 2 equiv of ferrocene to 2, or by the addition of 1 equiv of PPh3, which concomitantly yields OPPh3. In addition, complex 2 reacts with excess cyclohexene at -42°C to give 1. Complex 2 was also characterized by EPR spectroscopy, and all of the data are consistent with 2 being an antiferromagnetically coupled iron(IV)-oxo ?-cation-radical complex. Rapid-mixing stopped-flow UV-vis studies show that the low-temperature complex 2 is generated as a short-lived intermediate at room temperature.

AROMATIC FLUORINE DERIVATIVES LXXXVII. GENERATION OF PENTAFLUOROPHENYLFLUOROIODONIUM ION

Bardin, V. V.,Furin, G. G.,Yakobson, G. G.

, p. 1288 - 1291 (2007/10/02)

The pentafluoroiodonium ion C6F5IF+ was generated by the action of antimony pentafluoride on pentafluorophenyliodine difluoride at -30 deg.C.For the case of the reaction with pentafluorobenzene it was shown that this cation is a stronger electrophilic agent than previously known iodonium salts RR'I+.Under the influence of fluorosulfonic acid iodosylpentafluorobenzene probably forms a complex of the donor-acceptor type.

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