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14364-93-3

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14364-93-3 Usage

Uses

They are used as catalysts in organic reactions. It is used in chemical, organic Intermediates research. They are used as platinum group compounds for the preparation of materials suitable for industrial applications, mainly in electronics as coatings.

Check Digit Verification of cas no

The CAS Registry Mumber 14364-93-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,6 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 14364-93:
(7*1)+(6*4)+(5*3)+(4*6)+(3*4)+(2*9)+(1*3)=103
103 % 10 = 3
So 14364-93-3 is a valid CAS Registry Number.
InChI:InChI=1/3CH3.HI.Pt/h3*1H3;1H;/q;;;;+1/p-1/rC3H9IPt/c1-5(2,3)4/h1-3H3

14364-93-3 Well-known Company Product Price

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  • Alfa Aesar

  • (39286)  Iodotrimethylplatinum(IV)   

  • 14364-93-3

  • 0.5g

  • 1323.0CNY

  • Detail
  • Alfa Aesar

  • (39286)  Iodotrimethylplatinum(IV)   

  • 14364-93-3

  • 1g

  • 2185.0CNY

  • Detail

14364-93-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Iodotrimethylplatinum(IV)

1.2 Other means of identification

Product number -
Other names carbanide,iodoplatinum

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:14364-93-3 SDS

14364-93-3Relevant articles and documents

A convenient synthesis for a variety of methyl- and trifluoromethylplatinum complexes

Clark,Manzer

, p. C41-C42 (1972)

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Volatile fluorinated trimethylplatinum(IV) β-diketonates with pyridine: Synthesis, properties, and structure

Zharkova,Baidina,Igumenov

, p. 680 - 687 (2011)

Volatile fluorinated trimethylplatinum(IV) β-diketonates with pyridine (CH3)3Pt(CH3-CO-CH-CO-CF3)Py (I) and (CH3)3Pt(CF3-CO-CH-CO-CF3)Py (II) obtained from trifluoroacetylacetone and hexafluoroacetylacetone were studied. The synthesis, elemental analysis data, and IR spectra were described. X-Ray diffraction analysis was performed and the crystal structure was determined; the geometric characteristics of complexes I and II were obtained. Both structures are monomeric molecular structures. The molecules in the crystal are connected only by weak van der Waals forces. The coordination polyhedron of platinum in I and II is a slightly distorted octahedron. The shortest Pt...Pt distances are 6.639 A (for I) and 6.254 A (for II). The average P-O, Pt-N, and P-C distances are 2.157, 2.182, and 2.030 A, respectively. The deviations of the bond angles at Pt atoms from ideal values of 90° do not exceed 4.8°.

Weakly-coordinated stable platinum nanocrystals

Marquardt, Dorothea,Barthel, Juri,Braun, Markus,Ganter, Christian,Janiak, Christoph

, p. 7607 - 7615 (2013/01/15)

Stable platinum nanocrystals with small diameters (1.0-2.3 nm), that are stable for a long time, with narrow size distributions were easily and reproducibly prepared without any additional stabilizers in glycol, glycerol, the ionic liquids (ILs) 1-n-butyl-3-methyl-imidazolium tetrafluoroborate [BMIm][BF4] and N-butyl-N-trimethyl-ammonium bis(trifluoromethylsulfonyl)imide [N4111][NTf2] or diphenylmethane (CH2Ph2) by thermal, photolytic or microwave assisted decomposition of the organometallic precursor methylcyclopentadienyl-trimethylplatinum(iv), (MeCp)PtMe3. Decomposition of the easily dispensible, air and moisture stable organometallic Pt(iv) precursor (MeCp)PtMe3 leads to well defined, small, crystalline and longterm stable Pt-nanoparticle (Pt-NP) dispersions without any additional surface-capping ligands. The Pt-NP/IL dispersion was shown to be a highly active catalyst (TOF 96000 h-1 at 0.0125 mol% Pt and quantitative conversion) for the biphasic hydrosilylation of phenylacetylene with triethylsilane, to the distal and proximal products triethyl(2- and1-phenylvinyl)silane.

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