Cas 288613-60-5,[Ru(CO)N4C20H2(C2H5)4(CH3)4(C6H3(C(CH3)3)2)2][NiN4C20H2(C6H13)4(CH3)4C6H3(C(CH3)3)2C6H4C2P(C6H5)2]

288613-60-5

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Basic information

Product Name: [Ru(CO)N₄C₂₀H₂(C₂H₅)4(CH₃)4(C₆H₃(C(CH₃)3)2)2][NiN₄C₂₀H₂(C₆H₁₃)4(CH₃)4C₆H₃(C(CH₃)3)2C₆H₄C₂P(C₆H₅)2]
Synonyms:
CAS NO:288613-60-5
Molecular Formula:
Molecular Weight: 2214.77
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: [Ru(CO)N₄C₂₀H₂(C₂H₅)4(CH₃)4(C₆H₃(C(CH₃)3)2)2][NiN₄C₂₀H₂(C₆H₁₃)4(CH₃)4C₆H₃(C(CH₃)3)2C₆H₄C₂P(C₆H₅)2](CAS DataBase Reference)
NIST Chemistry Reference: [Ru(CO)N₄C₂₀H₂(C₂H₅)4(CH₃)4(C₆H₃(C(CH₃)3)2)2][NiN₄C₂₀H₂(C₆H₁₃)4(CH₃)4C₆H₃(C(CH₃)3)2C₆H₄C₂P(C₆H₅)2](288613-60-5)
EPA Substance Registry System: [Ru(CO)N₄C₂₀H₂(C₂H₅)4(CH₃)4(C₆H₃(C(CH₃)3)2)2][NiN₄C₂₀H₂(C₆H₁₃)4(CH₃)4C₆H₃(C(CH₃)3)2C₆H₄C₂P(C₆H₅)2](288613-60-5)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 288613-60-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 288613-60-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,8,6,1 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 288613-60:
(8*2)+(7*8)+(6*8)+(5*6)+(4*1)+(3*3)+(2*6)+(1*0)=175
175 % 10 = 5
So 288613-60-5 is a valid CAS Registry Number.

288613-60-5Upstream product

288613-60-5Downstream Products

288613-60-5Relevant academic research and scientific papers

Phosphine-substituted porphyrins as supramolecular building blocks

Darling, Scott L.,Stulz, Eugen,Feeder, Neil,Bampos, Nick,Sanders, Jeremy K. M.

, p. 261 - 264 (2007/10/03)

A route to alkyne-phosphine-substituted metalloporphyrins is presented. The X-ray structure of the methanol adduct of a diphenylphosphine Zn(II) porphyrin reveals solid state dimerisation accompanied by proton transfer from coordinated methanol to phosphine in a process reminiscent of carbonic anhydrase. The ability of the phosphine-substituted porphyrins to form non- covalent arrays with a Ru(II) porphyrin was explored using 1H/31P NMR and UV/vis spectroscopy as well as MALDI-TOF mass spectrometry.

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