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160262-01-1

[(η(6)-1-isopropyl-4-methylbenzene)Ru(2,2'-bipyridine)(H2O)](2+) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 160262-01-1 Structure

  • Basic information

    1. Product Name: [(η(6)-1-isopropyl-4-methylbenzene)Ru(2,2'-bipyridine)(H2O)](2+)
    2. Synonyms:
    3. CAS NO:160262-01-1
    4. Molecular Formula:
    5. Molecular Weight: 409.493
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 160262-01-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: [(η(6)-1-isopropyl-4-methylbenzene)Ru(2,2'-bipyridine)(H2O)](2+)(CAS DataBase Reference)
    10. NIST Chemistry Reference: [(η(6)-1-isopropyl-4-methylbenzene)Ru(2,2'-bipyridine)(H2O)](2+)(160262-01-1)
    11. EPA Substance Registry System: [(η(6)-1-isopropyl-4-methylbenzene)Ru(2,2'-bipyridine)(H2O)](2+)(160262-01-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 160262-01-1(Hazardous Substances Data)

160262-01-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 160262-01-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,2,6 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 160262-01:
(8*1)+(7*6)+(6*0)+(5*2)+(4*6)+(3*2)+(2*0)+(1*1)=91
91 % 10 = 1
So 160262-01-1 is a valid CAS Registry Number.

160262-01-1Upstream product

160262-01-1Downstream Products

160262-01-1Relevant articles and documents

Upconverting Nanoparticles Prompt Remote Near-Infrared Photoactivation of Ru(II)-Arene Complexes

Ruggiero, Emmanuel,Garino, Claudio,Mareque-Rivas, Juan C.,Habtemariam, Abraha,Salassa, Luca

, p. 2801 - 2811 (2016)

The synthesis and full characterisation (including X-ray diffraction studies and DFT calculations) of two new piano-stool RuII-arene complexes, namely [(η6-p-cym)Ru(bpy)(m-CCH-Py)][(PF)6]2 (1) and [(η6-p-cym)Ru(bpm)(m-CCH-Py)][(PF)6]2 (2; p-cym=p-cymene, bpy=2,2′-bipyridine, bpm=2,2′-bipyrimidine, and m-CCH-Py=3-ethynylpyridine), is described and discussed. The reaction of the m-CCH-Py ligand of 1 and 2 with diethyl-3-azidopropyl phosphonate by Cu-catalysed click chemistry affords [(η6-p-cym)Ru(bpy)(P-Trz-Py)][(PF)6]2 (3) and [(η6-p-cym)Ru(bpm)(P-Trz-Py)][(PF)6]2 (4; P-Trz-Py=[3-(1-pyridin-3-yl-[1,2,3]triazol-4-yl)-propyl]phosphonic acid diethyl ester). Upon light excitation at λ=395 nm, complexes 1-4 photodissociate the monodentate pyridyl ligand and form the aqua adduct ions [(η6-p-cym)Ru(bpy)(H2O)]2+ and [(η6-p-cym)Ru(bpm)(H2O)]2+. Thulium -doped upconverting nanoparticles (UCNPs) are functionalised with 4, thus exploiting their surface affinity for the phosphonate group in the complex. The so-obtained nanosystem UCNP@4 undergoes near-infrared (NIR) photoactivation at λ=980 nm, thus producing the corresponding reactive aqua species that binds the DNA-model base guanosine 5′-monophosphate.

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