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  • 1160044-49-4 Structure
  • Basic information

    1. Product Name: [Rh(mesBIAN)(CO)Cl]
    2. Synonyms:
    3. CAS NO:1160044-49-4
    4. Molecular Formula:
    5. Molecular Weight: 582.935
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1160044-49-4.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: [Rh(mesBIAN)(CO)Cl](CAS DataBase Reference)
    10. NIST Chemistry Reference: [Rh(mesBIAN)(CO)Cl](1160044-49-4)
    11. EPA Substance Registry System: [Rh(mesBIAN)(CO)Cl](1160044-49-4)
  • 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: 1160044-49-4(Hazardous Substances Data)

1160044-49-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1160044-49-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,0,0,4 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1160044-49:
(9*1)+(8*1)+(7*6)+(6*0)+(5*0)+(4*4)+(3*4)+(2*4)+(1*9)=104
104 % 10 = 4
So 1160044-49-4 is a valid CAS Registry Number.

1160044-49-4Upstream product

1160044-49-4Downstream Products

1160044-49-4Relevant articles and documents

Application of UV-Vis spectroscopy to high throughput screening of hydroamination catalysts

Kennedy, Danielle F.,Messerle, Barbara A.,Rumble, Sarah L.

, p. 818 - 824 (2009)

Potential catalysts for the hydroamination of 2-(2-phenylethynyl)aniline 2 which have been identified through high throughput screening methods were investigated. Two complexes were shown to be highly active hydroamination catalysts in acetone: the in situ combinations of [Rh(CO)2Cl] 2-mesBIAN-NaBF4 (mesBIAN = bis(2,4,6-trimethylphenylimino) acenapthene) and [Ir(COD)Cl]2-NaBF4 (COD = 1,5-cyclooctadiene). The isolated complexes [M(N-N)XCl]BF4 (M = Rh, Ir; N-N = bidentate nitrogen donor ligand; X = CO or Cp*) were found to be inactive as catalysts for the conversion of 2 to 3. However, chloride abstraction from these complexes through the addition of AgBF4 was found to generate extremely active catalysts. Particularly active was the complex [Rh(CO)ClmesBIAN]-AgBF4 (5 mol%) which achieved complete conversion of 2 to 3 in 12 minutes at 50 °C. Also identified was the formation of the unusual product, N-(2-methylvinyl)-2-phenylindole 5, catalysed by [IrCp*Cl2]2-NaBF4 from starting material 2via the incorporation of one molecule of acetone.

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