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1492022-71-5

[Ru(η5-Cp)(η5-4-(2-phenylethynyl)indene)] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1492022-71-5 Structure

  • Basic information

    1. Product Name: [Ru(η5-Cp)(η5-4-(2-phenylethynyl)indene)]
    2. Synonyms: [Ru(η5-Cp)(η5-4-(2-phenylethynyl)indene)]
    3. CAS NO:1492022-71-5
    4. Molecular Formula:
    5. Molecular Weight: 381.439
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1492022-71-5.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: [Ru(η5-Cp)(η5-4-(2-phenylethynyl)indene)](CAS DataBase Reference)
    10. NIST Chemistry Reference: [Ru(η5-Cp)(η5-4-(2-phenylethynyl)indene)](1492022-71-5)
    11. EPA Substance Registry System: [Ru(η5-Cp)(η5-4-(2-phenylethynyl)indene)](1492022-71-5)

  • 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: 1492022-71-5(Hazardous Substances Data)

1492022-71-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1492022-71-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,9,2,0,2 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1492022-71:
(9*1)+(8*4)+(7*9)+(6*2)+(5*0)+(4*2)+(3*2)+(2*7)+(1*1)=145
145 % 10 = 5
So 1492022-71-5 is a valid CAS Registry Number.

1492022-71-5Downstream Products

1492022-71-5Relevant articles and documents

Highly enantiomerically enriched planar chiral cyclopentadienyl(indenyl) ruthenium complexes

Wagschal, Simon,Mercier, Audrey,Kuendig, E. Peter

, p. 7133 - 7140 (2013)

The functionalization of highly enantiomerically enriched planar chiral cyclopentadienyl(4-bromoindenyl)ruthenium complexes is detailed. Lithium/bromine exchange followed by an electrophilic quench using N,N-dimethylformamide (DMF), trimethylsilyl chloride, benzaldehyde, acetone, or 1,2-diiodoethane afforded the corresponding enantiomerically enriched planar chiral complexes. Suzuki-Miyaura cross-coupling led to cyclopentadienyl(indenyl)ruthenium complexes bearing aryl and alkenyl groups in high yields. Similarly, in situ generation of the boronate intermediate using 9-MeO-9-BBN and a metalated species in the Suzuki-Miyaura reaction gave heteroaryl, alkynyl, and alkyl cyclopentadienyl(indenyl)ruthenium complexes with retention of configuration and enantiomeric excess.

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