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13462-90-3

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13462-90-3 Usage

Description

Nickel iodide is a chemical compound with the formula NiI2, which exists as a black, crystalline powder or blue-green crystals. It is hygroscopic, meaning it has the ability to absorb moisture from the surrounding environment, and is soluble in both alcohol and water.

Uses

1. Used in Chemical Synthesis:
Nickel iodide is used as a catalyst in the Sml2 mediated homocoupling of imines into vicinal diamines and heterocoupling reactions between imines and ketones. This application is crucial in the synthesis of various organic compounds and pharmaceuticals.
2. Used in Preparation of Nickel Complexes:
Nickel iodide is utilized in the preparation of nickel complexes for migratory reductive cross-coupling, a chemical reaction that involves the formation of new carbon-carbon or carbon-heteroatom bonds. This process is essential in the development of complex organic molecules and materials.

Preparation

Nickel iodide can be prepared by dehydration of the hexahydrate or by the metathetic reaction between sodium iodide and nickel(II) chloride or nitrate in ethanol. It has the CdCl2 type lattice and is paramagnetic down to 75°K. Only one hydrate is well characterized—the blue-green NiI2?6H20 ; unlike the other halide hexahydrates, this contains [Ni(H2O)6]2+ cations.

Hazard

Toxic by ingestion.

Check Digit Verification of cas no

The CAS Registry Mumber 13462-90-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,6 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13462-90:
(7*1)+(6*3)+(5*4)+(4*6)+(3*2)+(2*9)+(1*0)=93
93 % 10 = 3
So 13462-90-3 is a valid CAS Registry Number.
InChI:InChI=1/2HI.Ni/h2*1H;/q;;+2/p-2

13462-90-3 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Detail
  • Alfa Aesar

  • (22893)  Nickel(II) iodide, anhydrous, 99.5% (metals basis)   

  • 13462-90-3

  • 5g

  • 424.0CNY

  • Detail
  • Alfa Aesar

  • (22893)  Nickel(II) iodide, anhydrous, 99.5% (metals basis)   

  • 13462-90-3

  • 25g

  • 1795.0CNY

  • Detail
  • Aldrich

  • (400777)  Nickel(II)iodide  powder

  • 13462-90-3

  • 400777-5G

  • 439.92CNY

  • Detail
  • Aldrich

  • (400777)  Nickel(II)iodide  powder

  • 13462-90-3

  • 400777-25G

  • 1,423.89CNY

  • Detail
  • Aldrich

  • (466301)  Nickel(II)iodide  anhydrous, powder, 99.99% trace metals basis

  • 13462-90-3

  • 466301-1G

  • 1,151.28CNY

  • Detail

13462-90-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Nickel(II) iodide

1.2 Other means of identification

Product number -
Other names NICKEL IODIDE

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:13462-90-3 SDS

13462-90-3Relevant articles and documents

Crystal growth and properties of PbI2 doped with Fe and Ni

Rybak,Lun',Bordun,Omelyan

, p. 1124 - 1127 (2005)

A procedure is described for doping PbI2 single crystals with Fe and Ni during vapor-phase growth in a closed system in the presence of excess iodine. The rate of mass transport in the system and the doping level of the crystals are shown to be governed by the dopant content in the source material and the source temperature. The effect of Fe and Ni doping on the low-temperature (5 K) exciton photoluminescence spectrum of PbI2 is discussed.

The metal carbonyls

Blanchard, Arthur A.

, p. 311 - 317 (1941)

When the metal carbonyls were first discovered, their properties were startling because they seemed to violate nearly all the previously recognized generalizations of chemistry. Even to-day the existence of the carbonyls is not particularly emphasized in

The reduction of nickel(II) halides by trialkyl phosphites

Vinal, Richard S.,Reynolds

, p. 1062 - 1063 (1964)

-

Thermal studies of N(1)-isopropyl-2-methyl-1,2-propanediamine complexes of nickel(II)X2 [X = I(1-), CF3CO2(1-), 0.5SO4(2-) and 0.5SeO4(2-)] in the solid state

Pariya, Chandi,Ghosh, Ashutosh,Ray Chaudhuri, Nirmalendu

, p. 153 - 160 (1995)

The complexes NiL2X2.nH2O (L = N(1)-isopropyl-2-methyl-1,2-propanediamine; X = 0.5SO4(2-) when n = 0; X = I(1-) when n = 2; X = CF3CO2(1-) when N = 0 or 2 and X = 0.5SeO4(2-) when n = 0 or 3) have been synthesized and their thermal behaviour has been studied. All the hydrated complexes are yellow in colour and on heating lose water of hydration accompanied by a yellow light blue thermochromic transition, except in the case of the iodide complex, which retains the original yellow colour on dehydration. However, NiL2I2 undergoes an irreversible exothermic phase transition (166-193°C; ΔH = -7.5 kJ mol**-1) with change in colour from yellow to reddish yellow. NiL2(CF3CO2)2 shows a reversible phase transition (heating cycle, 144-170°C; ΔH = 3.1 kJ mol**-1; cooling cycle, 158-135°C; ΔH = -3.1 kJ mol**-1) with no visual change in colour. All the yellow complexes posses square-planargeometry and the light blue complexes NiL2X2 (X = CF3CO2(1-), 0.5SO4(2- ) and 0.5SeO4(2-)) are expected to be pentaccordinated. The phase transition occuring in NiL2X2 (X = I(1-) and CF3CO2(1-)) is due to conformational changes of the diamine chelate rings.

Asymmetric reduction and hydrogenation over heterogeneous catalysts prepared by reacting nickel-boride with norephedrine

Court,Molvinger,Lopez

, p. 267 - 273 (1999)

Nanoparticles of NiB2 were prepared by reducing nickel iodide with lithium borohydride in anhydrous oxygen-free THF. The hydroxy group and the amino-group of norephedrine reacted with boron atoms, evolving 1 mol of hydrogen for each mole of amino alcohol to afford a chiral oxazaborolidine anchored at the surface of the particles. The reduction of acetophenone utilizing borane-THF as reducing agent in the presence of 1 equivalent of NiB2 bound oxazaborolidine afforded 1-phenylethanol was excellent enantioselectivity (ee). The oxazaborolidine was strongly bound to the particles since the catalyst could be recycled at least two times with no performance loss. The catalyst hydrogenated 4-methylpentan-2-one, isophorone, and acetophenone, into 4-methyl-pentan-2-ol, dihydroisophorone, and 1-phenylethanol, respectively, in any case the S configuration predominated slightly. The ee was constant when the catalyst was reused. The catalytic hydrogenation over an oxazaborolidine boron bound to Ni particles was not useful in the enantioselective synthesis of alcohol.

Second harmonic generation in boracites

Zagudailova,Plachinda,Berdonosov,Stefanovich,Dolgikh

, p. 393 - 396 (2008/10/09)

The M3B7O13X (M=Mg, Ni, Cd; X=Cl, Br, I) boracites were synthesized and characterized by x-ray diffraction and second harmonic generation. Their nonlinear optical susceptibility was estimated using the Phillips-Van Vechten

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