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37216-50-5

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37216-50-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37216-50-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,2,1 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 37216-50:
(7*3)+(6*7)+(5*2)+(4*1)+(3*6)+(2*5)+(1*0)=105
105 % 10 = 5
So 37216-50-5 is a valid CAS Registry Number.

37216-50-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name octadecacarbonylhexaosmium

1.2 Other means of identification

Product number -
Other names -

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:37216-50-5 SDS

37216-50-5Relevant articles and documents

Synthesis of High Nuclearity Cluster Alkynes Under Mild Reaction Conditions; the X-Ray Crystal Structures of , , and

Gomez-Sal, M. Pilar,Johnson, Brian F. G.,kamarudin, Rose A.,Lewis, Jack,Raithby, Paul R.

, p. 1622 - 1625 (1985)

Reaction of the labilised cluster with the terminal alkynes HCCR (R = Me, Et, or Ph) affords the isomeric alkyne substituted clusters and R = Me (2), Et

Synthesis, Reactivity, and X-Ray Crystal Structures of CH2Cl2 and . Model Compounds for C-H Activation

Couture, Christiane,Farrar, David H.

, p. 2253 - 2260 (2007/10/02)

The reaction of with (C8H12=cyclo-octa-1,5-diene) results in the formation of (1).The geometry of (1) may be derived from that of by bridging one edge of the central Os tetrahedron with one Pt atom of the dimer unit Pt2(μ-C8H10)(C8H12).One C8H12 group has been dehydrogenated to C8H10 and the two resulting hydride ligands are terminally bound to different metals of the Os6 core.The C8H10 ligand is bound in an η3-allyl fashion to one Pt atom and by an η2-olefinic bond and ?-alkyl bond to the second Pt atom.Upon heating in toluene, complex (1) rearranges to the known complex (3).Complex (3) is without hydride ligands and possesses a geometry of two edge-fused Os tetrahedra, one of which is Pt-bicapped.The complex (2) was isolated from the reaction of with C8H12.Complex (2) has the bicapped tetrahedral geometry of with the μ-C8H11 group bridging two Os atoms of the central tetrahedron.The hydride ligand caps a triangulated Os face.This complex reacts with CO to afford the parent cluster .

SYNTHESIS AND X-RAY ANALYSIS OF AND

Johnson, Brian F.G.,Lewis, Jack,Nelson, William J.H.,Vargas, Maria D.,Braga, Dario,at al.

, p. 2151 - 2162 (2007/10/02)

The cluster anion -(1) has been obtained from the reaction of in BuiOH and X-ray analysis of its + salt shows that the anion has an unusual fused tetrahedral metal-core geometry related to that of .Reaction of (1) with iodine gives (2) in which an overall change in cluster geometry has occurred; the reaction is reversible and heating (2) with iodide regenerates (1).Reaction of (1) with concentrated H2SO4 gives which reacts with P(OMe)3 to give > and with halide ions to give evantually 2-.Crystals of are triclinic, space group P, with a = 16.775(3), b = 13.509(2), c = 11.267(2) Angstroem, α = 89.88(1), β = 103.97(1), γ = 96.99(1)deg, and Z = 2.Refinement of atomic parameters using 5 615 absorption-corrected data converged at R = 0.0359.Crystals of *H2O are monoclinic, space group P21/c, with a = 14.386(2), b = 11.037(1), c = 24.629(3) Angstroem, β = 94.30(2)deg, and Z = 4.Refinement of atomic parameters using 4 644 absorptioncorrected reflections converged at R = 0.0569.

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